A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526056



Internal ID15453349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:4146466..4174554hg38UCSC Ensembl
Innerchr2:4194056..4222144hg19UCSC Ensembl
Innerchr2:4171931..4200019hg18UCSC Ensembl
Innerchr2:3687425..3715513hg17UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3828089
hg1928089
hg1828089
hg1728089
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702294
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526056
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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