A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv656176



Internal ID15392828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:19815811..19822598hg38UCSC Ensembl
Innerchr7:19855434..19862221hg19UCSC Ensembl
Innerchr7:19821959..19828746hg18UCSC Ensembl
Innerchr7:19628674..19635461hg17UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg386788
hg196788
hg186788
hg176788
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519430
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv656176
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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