A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030737



Internal ID18773268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31385103..31489856hg38UCSC Ensembl
Innerchr6:31352880..31457633hg19UCSC Ensembl
Innerchr6:31460859..31565612hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg38104754
hg19104754
hg18104754
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5942n100
Supporting Variantsnssv3655782, nssv3655783
Samples
Known GenesHCG26, HCP5, MICA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1030737
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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