A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521882



Internal ID15102489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:23383982..23388172hg38UCSC Ensembl
Innerchr1:23710475..23714665hg19UCSC Ensembl
Innerchr1:23583062..23587252hg18UCSC Ensembl
Innerchr1:23455781..23459971hg17UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg384191
hg194191
hg184191
hg174191
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694653
Samples
Known GenesTCEA3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521882
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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