A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524122



Internal ID15451415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:135626651..135739111hg38UCSC Ensembl
Innerchr3:135345493..135457953hg19UCSC Ensembl
Innerchr3:136828183..136940643hg18UCSC Ensembl
Innerchr3:136828191..136940651hg17UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg38112461
hg19112461
hg18112461
hg17112461
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700000
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524122
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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