A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3648876



Internal ID18947157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:82010915..82022608hg38UCSC Ensembl
Innerchr6:82720632..82732325hg19UCSC Ensembl
Innerchr6:82777351..82789044hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3811694
hg1911694
hg1811694
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1020783
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3648876
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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