A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv692600



Internal ID15082566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:24224894..24376124hg38UCSC Ensembl
Innerchr7:24264513..24415743hg19UCSC Ensembl
Innerchr7:24231038..24382268hg18UCSC Ensembl
Innerchr7:24037753..24188983hg17UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38151231
hg19151231
hg18151231
hg17151231
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)nssv692600
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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