A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520908



Internal ID15448201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:174083961..174816144hg38UCSC Ensembl
Innerchr3:173801751..174533934hg19UCSC Ensembl
Innerchr3:175284445..176016628hg18UCSC Ensembl
Innerchr3:175284453..176016636hg17UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg38732184
hg19732184
hg18732184
hg17732184
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697682
Samples
Known GenesNLGN1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520908
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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