A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700360



Internal ID15437012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:23858704..23978379hg38UCSC Ensembl
Innerchr6:23858932..23978607hg19UCSC Ensembl
Innerchr6:23966911..24086586hg18UCSC Ensembl
Innerchr6:23966911..24086586hg17UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg38119676
hg19119676
hg18119676
hg17119676
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524433
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700360
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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