A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697588



Internal ID15087554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:40292919..40385541hg38UCSC Ensembl
Innerchr7:40332518..40425140hg19UCSC Ensembl
Innerchr7:40299043..40391665hg18UCSC Ensembl
Innerchr7:40105758..40198380hg17UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3892623
hg1992623
hg1892623
hg1792623
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520748
Supporting Variants
Samples
Known GenesC7orf10
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697588
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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