A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525335



Internal ID15452628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:84909926..84914831hg38UCSC Ensembl
Innerchr3:84959077..84963982hg19UCSC Ensembl
Innerchr3:85041767..85046672hg18UCSC Ensembl
Innerchr3:85041767..85046672hg17UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg384906
hg194906
hg184906
hg174906
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701450
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525335
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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