A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516761



Internal ID15444054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:117248107..117252792hg38UCSC Ensembl
Innerchr7:116888161..116892846hg19UCSC Ensembl
Innerchr7:116675397..116680082hg18UCSC Ensembl
Innerchr7:116482112..116486797hg17UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg384686
hg194686
hg184686
hg174686
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv670665, nssv658080
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516761
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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