A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516477



Internal ID15443770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:69507769..69523816hg38UCSC Ensembl
Innerchr6:70217661..70233708hg19UCSC Ensembl
Innerchr6:70274382..70290429hg18UCSC Ensembl
Innerchr6:70274382..70290429hg17UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3816048
hg1916048
hg1816048
hg1716048
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv385n21
Supporting Variantsnssv692737, nssv679096, nssv661699, nssv685314, nssv668600, nssv690802, nssv662060, nssv691239, nssv672335, nssv693172, nssv671594, nssv659207, nssv673170
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516477
Frequency
Sample Size2026
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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