A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520501



Internal ID15447794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:164115200..164244697hg38UCSC Ensembl
Innerchr3:163832988..163962485hg19UCSC Ensembl
Innerchr3:165315682..165445179hg18UCSC Ensembl
Innerchr3:165315690..165445187hg17UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38129498
hg19129498
hg18129498
hg17129498
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697457
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520501
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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