A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521906



Internal ID15449199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:169944298..169948644hg38UCSC Ensembl
Innerchr3:169662086..169666432hg19UCSC Ensembl
Innerchr3:171144780..171149126hg18UCSC Ensembl
Innerchr3:171144788..171149134hg17UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg384347
hg194347
hg184347
hg174347
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694678
Samples
Known GenesLOC100128164
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521906
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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