A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704541



Internal ID15441193
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528013
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704541
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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