A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv913921



Internal ID16207877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:89004736..90277942hg38UCSC Ensembl
Innerchr2:89304233..90316801hg19UCSC Ensembl
Innerchr2:89085348..89954106hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg381273207
hg191012569
hg18868759
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv582392
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv913921
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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