A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022664



Internal ID19111882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:76293455..76318052hg38UCSC Ensembl
Innerchr6:77003172..77027769hg19UCSC Ensembl
Innerchr6:77059892..77084489hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3824598
hg1924598
hg1824598
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6017n100
Supporting Variantsnssv3658825
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)nsv1022664
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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