Variant Details

Variant: esv3305062

Internal ID

15152010

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr4:28319129..28319130	hg38	UCSC Ensembl
Inner	chr4:28319111..28319148	hg38	UCSC Ensembl
Outer	chr4:28319110..28319149	hg38	UCSC Ensembl
	chr4:28320751..28320752	hg19	UCSC Ensembl
Inner	chr4:28320733..28320770	hg19	UCSC Ensembl
Outer	chr4:28320732..28320771	hg19	UCSC Ensembl
	chr4:27929849..27929850	hg18	UCSC Ensembl
Inner	chr4:27929868..27929831	hg18	UCSC Ensembl
Outer	chr4:27929830..27929869	hg18	UCSC Ensembl

Cytoband

4p15.1

Allele length

Assembly	Allele length
hg38	297
hg19	297
hg18	297

Variant Type

CNV mobile element insertion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv7781686, essv7809080, essv7799979, essv7822651, essv7798112, essv7778307, essv7780027, essv7827735, essv7814805, essv7790297, essv7830179, essv7780831, essv7773884, essv7775840, essv7785372, essv7788891, essv7808540, essv7784041, essv7835080, essv7796805, essv7826599, essv7807838, essv7815321, essv7783378, essv7797400, essv7787062, essv7773307, essv7771965, essv7826421, essv7822389, essv7830576, essv7834648, essv7831094, essv7795888, essv7794827, essv7788104, essv7835758, essv7780332, essv7798435, essv7836077, essv7829349, essv7793351

Samples

NA18592, NA12414, NA18561, NA11931, NA18526, NA19005, NA18940, NA12891, NA18960, NA18942, NA11992, NA12287, NA18964, NA18949, NA12761, NA18970, NA18520, NA18638, NA11993, NA18951, NA18605, NA12878, NA18579, NA18572, NA18948, NA11919, NA11894, NA18555, NA18570, NA18593, NA12043, NA18608, NA11881, NA18961, NA07051, NA12763, NA06986, NA12749, NA18609, NA18552, NA12006, NA18965

Known Genes

Method

Sequencing

Analysis

Platform

Roche 454

Comments

Reference

1000_Genomes_Consortium_Pilot_Project

Pubmed ID

20981092

Accession Number(s)

esv3305062

Frequency

Sample Size	185
Observed Gain	42
Observed Loss	0
Observed Complex	0
Frequency	n/a