A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704858



Internal ID15094824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:57309358..57349862hg38UCSC Ensembl
Innerchr7:57377065..57417569hg19UCSC Ensembl
Innerchr7:57381007..57421511hg18UCSC Ensembl
Innerchr7:57187722..57228226hg17UCSC Ensembl
Cytoband7p11.1
Allele length
AssemblyAllele length
hg3840505
hg1940505
hg1840505
hg1740505
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520659
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704858
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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