Variant Details

Variant: esv3304195

Internal ID

14804457

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr3:191281661..191281662	hg38	UCSC Ensembl
Inner	chr3:191281644..191281679	hg38	UCSC Ensembl
Outer	chr3:191281643..191281680	hg38	UCSC Ensembl
	chr3:190999450..190999451	hg19	UCSC Ensembl
Inner	chr3:190999433..190999468	hg19	UCSC Ensembl
Outer	chr3:190999432..190999469	hg19	UCSC Ensembl
	chr3:192482144..192482145	hg18	UCSC Ensembl
Inner	chr3:192482162..192482127	hg18	UCSC Ensembl
Outer	chr3:192482126..192482163	hg18	UCSC Ensembl

Cytoband

3q28

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

essv7824643, essv7792318, essv7795825, essv7781638, essv7813331, essv7789201, essv7829653, essv7771868, essv7813835, essv7806617, essv7796479, essv7773469, essv7834932, essv7819443, essv7770796, essv7772438, essv7772954, essv7831183, essv7820421, essv7782811, essv7777588, essv7827966, essv7809919, essv7796901, essv7825646, essv7816823, essv7803531, essv7782520, essv7822281, essv7799305, essv7808844, essv7797718, essv7815272, essv7806079, essv7774671, essv7785818, essv7793749, essv7783370, essv7792700, essv7783778, essv7809201, essv7826323, essv7834115, essv7784491, essv7773932, essv7790349, essv7778442, essv7821481, essv7771380, essv7779180, essv7779382, essv7817427, essv7791367, essv7801244, essv7794125, essv7824451, essv7788921, essv7823194, essv7834730, essv7780573, essv7780795, essv7785018, essv7829392, essv7831576, essv7832830, essv7821876, essv7800272, essv7827176, essv7826792, essv7803164, essv7828956, essv7835505, essv7805193, essv7808566, essv7786786, essv7807938, essv7775313, essv7815133, essv7800978, essv7825964, essv7799550, essv7788133, essv7775435, essv7827687, essv7787722, essv7817066, essv7811637, essv7836215, essv7776572

Samples

NA12717, NA11995, NA11829, NA18861, NA18508, NA10851, NA11920, NA11931, NA12751, NA18959, NA18870, NA12750, NA12155, NA07346, NA18563, NA19005, NA18944, NA18940, NA12812, NA18960, NA11992, NA11918, NA18571, NA12287, NA18949, NA12761, NA18970, NA12156, NA19238, NA12044, NA11994, NA12815, NA18520, NA19239, NA18973, NA11993, NA11831, NA10847, NA18951, NA18605, NA12489, NA12003, NA12878, NA12872, NA18579, NA18572, NA18907, NA18537, NA18573, NA11919, NA11894, NA12249, NA18912, NA12892, NA18853, NA19099, NA19257, NA18555, NA12144, NA18523, NA18570, NA18593, NA18576, NA12043, NA18608, NA12716, NA11881, NA19108, NA18961, NA18952, NA18564, NA19240, NA12873, NA12874, NA07037, NA12763, NA06986, NA19143, NA12749, NA18609, NA18552, NA18505, NA19129, NA12006, NA12154, NA18562, NA12776, NA18965, NA18577

Known Genes

UTS2B

Method

Sequencing

Analysis

Platform

Roche 454

Comments

Reference

1000_Genomes_Consortium_Pilot_Project

Pubmed ID

20981092

Accession Number(s)

esv3304195

Frequency

Sample Size	185
Observed Gain	89
Observed Loss	0
Observed Complex	0
Frequency	n/a