A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv913926



Internal ID16207882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:89026617..90226525hg38UCSC Ensembl
Innerchr2:89326114..90265391hg19UCSC Ensembl
Innerchr2:89107229..89902696hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg381199909
hg19939278
hg18795468
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv582396
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)nssv913926
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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