A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519964



Internal ID15447257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:51977196..52299016hg38UCSC Ensembl
Innerchr7:52044892..52366712hg19UCSC Ensembl
Innerchr7:52012386..52334206hg18UCSC Ensembl
Innerchr7:51819101..52140921hg17UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg38321821
hg19321821
hg18321821
hg17321821
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697151
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519964
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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