A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524443



Internal ID15451736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:11884493..11958321hg38UCSC Ensembl
Innerchr3:11925967..11999795hg19UCSC Ensembl
Innerchr3:11900967..11974795hg18UCSC Ensembl
Innerchr3:11900967..11974795hg17UCSC Ensembl
Cytoband3p25.2
Allele length
AssemblyAllele length
hg3873829
hg1973829
hg1873829
hg1773829
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700375
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524443
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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