A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv653693



Internal ID15043659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:24229586..24386936hg38UCSC Ensembl
Innerchr7:24269205..24426555hg19UCSC Ensembl
Innerchr7:24235730..24393080hg18UCSC Ensembl
Innerchr7:24042445..24199795hg17UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38157351
hg19157351
hg18157351
hg17157351
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517053
Supporting Variants
Samples
Known GenesNPY
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv653693
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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