A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520805



Internal ID15101412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:119640198..119642568hg38UCSC Ensembl
Innerchr3:119359045..119361415hg19UCSC Ensembl
Innerchr3:120841735..120844105hg18UCSC Ensembl
Innerchr3:120841735..120844105hg17UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg382371
hg192371
hg182371
hg172371
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697622
Samples
Known GenesPOPDC2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520805
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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