A curated catalogue of human genomic structural variation

Variant Details

Variant: nsv572719

Internal ID

16360128

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr16:57332466..57333135	hg38	UCSC Ensembl
Inner	chr16:57366378..57367047	hg19	UCSC Ensembl
Inner	chr16:55923879..55924548	hg18	UCSC Ensembl

Cytoband

16q13

Allele length

Assembly	Allele length
hg38	670
hg19	670
hg18	670

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

M

Merged Variants

Supporting Variants

nssv857913, nssv857789, nssv857815, nssv857822, nssv857821, nssv857907, nssv857831, nssv857890, nssv857866, nssv857799, nssv857906, nssv857869, nssv857830, nssv857887, nssv857875, nssv857919, nssv857820, nssv857814, nssv857846, nssv857865, nssv857856, nssv857895, nssv857804, nssv857845, nssv857917, nssv857880, nssv857840, nssv857903, nssv857918, nssv857835, nssv857878, nssv857864, nssv857824, nssv857783, nssv857908, nssv857901, nssv857826, nssv857818, nssv857792, nssv857898, nssv857802, nssv857843, nssv857816, nssv857896, nssv857805, nssv857813, nssv857860, nssv857914, nssv857801, nssv857791, nssv857842, nssv857884, nssv857790, nssv857897, nssv857839, nssv857910, nssv857882, nssv857892, nssv857863, nssv857885, nssv857837, nssv857876, nssv857819, nssv857788, nssv857874, nssv857861, nssv857787, nssv857850, nssv857785, nssv857849, nssv857817, nssv857807, nssv857847, nssv857793, nssv857893, nssv857811, nssv857798, nssv857853, nssv857879, nssv857905, nssv857883, nssv857858, nssv857857, nssv857852, nssv857841, nssv857786, nssv857909, nssv857800, nssv857784, nssv857851, nssv857796, nssv857828, nssv857921, nssv857809, nssv857825, nssv857806, nssv857827, nssv857889, nssv857870, nssv857881, nssv857868, nssv857812, nssv857912, nssv857867, nssv857862, nssv857836, nssv857823, nssv857844, nssv857803, nssv857855, nssv857886, nssv857871, nssv857838, nssv857829, nssv857810, nssv857832, nssv857904, nssv857902, nssv857859, nssv857916, nssv857915, nssv857872, nssv857911, nssv857873, nssv857794, nssv857894, nssv857899, nssv857834, nssv857854, nssv857808, nssv857795, nssv857891, nssv857833, nssv857797, nssv857920, nssv857877, nssv857888, nssv857848, nssv857900

Samples

Known Genes

Method

SNP array

Analysis

Illumina SNP array copy number analysis

Platform

Not reported

Comments

Reference

Cooper_et_al_2011

Pubmed ID

Accession Number(s)

Frequency

Sample Size	17421
Observed Gain	0
Observed Loss	139
Observed Complex	0
Frequency	n/a