A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520600



Internal ID15101207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:23245342..23253189hg38UCSC Ensembl
Innerchr7:23284961..23292808hg19UCSC Ensembl
Innerchr7:23251486..23259333hg18UCSC Ensembl
Innerchr7:23058201..23066048hg17UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg387848
hg197848
hg187848
hg177848
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694390
Samples
Known GenesGPNMB
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520600
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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