A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701076



Internal ID15091042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:89838804..89854530hg38UCSC Ensembl
Innerchr7:89468118..89483844hg19UCSC Ensembl
Innerchr7:89306054..89321780hg18UCSC Ensembl
Innerchr7:89112769..89128495hg17UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3815727
hg1915727
hg1815727
hg1715727
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515995
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701076
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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