A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv668689



Internal ID15405341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:129261588..129405350hg38UCSC Ensembl
Innerchr7:128901429..129045191hg19UCSC Ensembl
Innerchr7:128688665..128832427hg18UCSC Ensembl
Innerchr7:128495380..128639142hg17UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg38143763
hg19143763
hg18143763
hg17143763
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516498
Supporting Variants
Samples
Known GenesAHCYL2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv668689
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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