A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601910



Internal ID16389319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31393647..31483699hg38UCSC Ensembl
Innerchr6:31361424..31451476hg19UCSC Ensembl
Innerchr6:31469403..31559455hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3890053
hg1990053
hg1890053
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10453n54
Supporting Variantsnssv1154288, nssv1154289, nssv1154286, nssv1154287, nssv1154291, nssv1154290
SamplesHGDP01208, 1780862101_A, HGDP00689, HGDP00975, HGDP00733, 1780862094_A
Known GenesHCG26, HCP5, MICA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601910
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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