A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523534



Internal ID15450827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:59273317..59302489hg38UCSC Ensembl
Innerchr3:59259043..59288215hg19UCSC Ensembl
Innerchr3:59234083..59263255hg18UCSC Ensembl
Innerchr3:59234083..59263255hg17UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3829173
hg1929173
hg1829173
hg1729173
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699309
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523534
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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