A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528013



Internal ID15455306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:147918934..147923378hg38UCSC Ensembl
Innerchr5:147298497..147302941hg19UCSC Ensembl
Innerchr5:147278690..147283134hg18UCSC Ensembl
Innerchr5:147278690..147283134hg17UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg384445
hg194445
hg184445
hg174445
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv357n21
Supporting Variantsnssv704541
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528013
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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