A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601908



Internal ID16042631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31393647..31482217hg38UCSC Ensembl
Innerchr6:31361424..31449994hg19UCSC Ensembl
Innerchr6:31469403..31557973hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3888571
hg1988571
hg1888571
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10453n54
Supporting Variantsnssv1154284
SamplesHGDP01223
Known GenesHCG26, HCP5, MICA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601908
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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