A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521135



Internal ID15101742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:217956863..217959727hg38UCSC Ensembl
Innerchr2:218821586..218824450hg19UCSC Ensembl
Innerchr2:218529831..218532695hg18UCSC Ensembl
Innerchr2:218647092..218649956hg17UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg382865
hg192865
hg182865
hg172865
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697808
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521135
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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