A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517632



Internal ID15444925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:155239158..155295574hg38UCSC Ensembl
Innerchr4:156160310..156216726hg19UCSC Ensembl
Innerchr4:156379760..156436176hg18UCSC Ensembl
Innerchr4:156517915..156574331hg17UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3856417
hg1956417
hg1856417
hg1756417
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv662577, nssv675674, nssv656252, nssv695967, nssv692193, nssv683524, nssv652603, nssv673227, nssv677965, nssv688748, nssv671108, nssv656734, nssv658443
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517632
Frequency
Sample Size2026
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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