A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516094



Internal ID15443387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:98111891..98176366hg38UCSC Ensembl
Innerchr5:97447595..97512070hg19UCSC Ensembl
Innerchr5:97473351..97537826hg18UCSC Ensembl
Innerchr5:97473351..97537826hg17UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3864476
hg1964476
hg1864476
hg1764476
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv671480, nssv666953, nssv666163
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516094
Frequency
Sample Size2026
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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