A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023876



Internal ID18766409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31398092..31483699hg38UCSC Ensembl
Innerchr6:31365869..31451476hg19UCSC Ensembl
Innerchr6:31473848..31559455hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3885608
hg1985608
hg1885608
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5943n100
Supporting Variantsnssv3655888, nssv3655887
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)nsv1023876
Frequency
Sample Size29084
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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