A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697379



Internal ID15434031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:40332994..40387401hg38UCSC Ensembl
Innerchr7:40372593..40427000hg19UCSC Ensembl
Innerchr7:40339118..40393525hg18UCSC Ensembl
Innerchr7:40145833..40200240hg17UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3854408
hg1954408
hg1854408
hg1754408
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520374
Supporting Variants
Samples
Known GenesC7orf10
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697379
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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