A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523699



Internal ID15450992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:72266805..72268319hg38UCSC Ensembl
Innerchr3:72315956..72317470hg19UCSC Ensembl
Innerchr3:72398646..72400160hg18UCSC Ensembl
Innerchr3:72398646..72400160hg17UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg381515
hg191515
hg181515
hg171515
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699506
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523699
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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