A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516049



Internal ID15096656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:71561478..71815314hg38UCSC Ensembl
Innerchr7:71026463..71280299hg19UCSC Ensembl
Innerchr7:70664399..70918235hg18UCSC Ensembl
Innerchr7:70471114..70724950hg17UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg38253837
hg19253837
hg18253837
hg17253837
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv665884, nssv656421, nssv689776
Samples
Known GenesCALN1, WBSCR17
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516049
Frequency
Sample Size2026
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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