A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697030



Internal ID15086996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:158875884..159257090hg38UCSC Ensembl
Innerchr7:158668575..159049780hg19UCSC Ensembl
Innerchr7:158361336..158742541hg18UCSC Ensembl
Innerchr7:158168051..158549256hg17UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38381207
hg19381206
hg18381206
hg17381206
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519749
Supporting Variants
Samples
Known GenesLINC00689, VIPR2, WDR60
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697030
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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