A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022776



Internal ID19111994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:94040460..94496222hg38UCSC Ensembl
Innerchr6:94750178..95205940hg19UCSC Ensembl
Innerchr6:94806899..95262661hg18UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38455763
hg19455763
hg18455763
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6094n100
Supporting Variantsnssv3648988
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)nsv1022776
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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