A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv657362



Internal ID15047328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:90482430..90537591hg38UCSC Ensembl
Innerchr7:90111744..90166905hg19UCSC Ensembl
Innerchr7:89949680..90004841hg18UCSC Ensembl
Innerchr7:89756395..89811556hg17UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3855162
hg1955162
hg1855162
hg1755162
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515998
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv657362
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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