A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527639



Internal ID15454932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:15726969..15755942hg38UCSC Ensembl
Innerchr7:15766594..15795567hg19UCSC Ensembl
Innerchr7:15733119..15762092hg18UCSC Ensembl
Innerchr7:15539834..15568807hg17UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3828974
hg1928974
hg1828974
hg1728974
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704108
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527639
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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