A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516808



Internal ID15444101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:72460275..72460843hg38UCSC Ensembl
Innerchr5:71756102..71756670hg19UCSC Ensembl
Innerchr5:71791858..71792426hg18UCSC Ensembl
Innerchr5:71791858..71792426hg17UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg38569
hg19569
hg18569
hg17569
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv672640, nssv687416, nssv656789, nssv674181, nssv690274, nssv676879, nssv658981, nssv671066, nssv678281, nssv673720, nssv676700
Samples
Known GenesZNF366
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516808
Frequency
Sample Size2026
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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