A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528569



Internal ID15455862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:103040269..103139958hg38UCSC Ensembl
Innerchr2:103656727..103756416hg19UCSC Ensembl
Innerchr2:103023159..103122848hg18UCSC Ensembl
Innerchr2:103115245..103214934hg17UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg3899690
hg1999690
hg1899690
hg1799690
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705188
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528569
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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