Variant Details

Variant: esv3304835

Internal ID

15151783

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr5:170774319..170774320	hg38	UCSC Ensembl
Inner	chr5:170774302..170774337	hg38	UCSC Ensembl
Outer	chr5:170774301..170774338	hg38	UCSC Ensembl
	chr5:170201323..170201324	hg19	UCSC Ensembl
Inner	chr5:170201306..170201341	hg19	UCSC Ensembl
Outer	chr5:170201305..170201342	hg19	UCSC Ensembl
	chr5:170133901..170133902	hg18	UCSC Ensembl
Inner	chr5:170133919..170133884	hg18	UCSC Ensembl
Outer	chr5:170133883..170133920	hg18	UCSC Ensembl

Cytoband

5q35.1

Allele length

Assembly	Allele length
hg38	294
hg19	294
hg18	294

Variant Type

CNV mobile element insertion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv7779228, essv7831109, essv7786064, essv7803574, essv7813523, essv7810278, essv7777802, essv7792751, essv7807836, essv7783335, essv7794594, essv7770487, essv7786356, essv7781752, essv7791542, essv7772727, essv7824605, essv7811152, essv7794961, essv7819233, essv7827872, essv7805617, essv7804671, essv7830659, essv7821026, essv7836488, essv7821682, essv7829973, essv7824256, essv7798636, essv7816227, essv7771392, essv7814642, essv7823426, essv7831277, essv7820748, essv7783101, essv7814232, essv7830421, essv7806949, essv7801558, essv7803826, essv7815953, essv7813376, essv7779755, essv7773523, essv7828357, essv7820243, essv7794174, essv7809881, essv7782250, essv7802394, essv7775773, essv7830196, essv7792080, essv7825664, essv7795841, essv7828658, essv7773741, essv7818170, essv7835574, essv7772689, essv7827083, essv7817049, essv7799845, essv7797754, essv7812637, essv7826100, essv7829169, essv7790426, essv7778358, essv7822549, essv7784131, essv7780565, essv7789748, essv7807521, essv7793276, essv7816650, essv7787311, essv7802750, essv7774914, essv7781168, essv7815306, essv7796228, essv7801008, essv7796498, essv7809289, essv7799411, essv7795255, essv7780239, essv7812362, essv7811603, essv7797278, essv7832263, essv7784979, essv7783918, essv7832673, essv7825354, essv7785390

Samples

NA18502, NA19141, NA12717, NA18947, NA11995, NA18861, NA18592, NA18508, NA10851, NA18561, NA11931, NA12045, NA12751, NA18545, NA19190, NA18870, NA18526, NA18510, NA12750, NA18969, NA07346, NA18563, NA19005, NA18944, NA18550, NA18519, NA12812, NA18489, NA12891, NA18558, NA18960, NA18942, NA18916, NA11992, NA18571, NA19138, NA18964, NA18949, NA12761, NA19238, NA11994, NA19239, NA12828, NA18638, NA11993, NA11831, NA10847, NA18951, NA18605, NA12003, NA12878, NA12872, NA18516, NA18579, NA18871, NA18572, NA12234, NA18907, NA18537, NA18566, NA18573, NA19114, NA11919, NA18499, NA11840, NA18856, NA12892, NA19257, NA18555, NA19225, NA12144, NA18523, NA18570, NA18593, NA18576, NA18542, NA12716, NA18909, NA19108, NA18961, NA18952, NA19147, NA18517, NA18564, NA19240, NA07051, NA18943, NA07037, NA19143, NA18501, NA19093, NA18609, NA19102, NA19116, NA18505, NA12006, NA18562, NA18965, NA18577

Known Genes

Method

Sequencing

Analysis

Platform

Roche 454

Comments

Reference

1000_Genomes_Consortium_Pilot_Project

Pubmed ID

20981092

Accession Number(s)

esv3304835

Frequency

Sample Size	185
Observed Gain	99
Observed Loss	0
Observed Complex	0
Frequency	n/a