A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv665884



Internal ID15055850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:71570435..71815314hg38UCSC Ensembl
Innerchr7:71035420..71280299hg19UCSC Ensembl
Innerchr7:70673356..70918235hg18UCSC Ensembl
Innerchr7:70480071..70724950hg17UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg38244880
hg19244880
hg18244880
hg17244880
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516049
Supporting Variants
Samples
Known GenesCALN1, WBSCR17
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv665884
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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