A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv906903



Internal ID16200859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:40879880..40987051hg38UCSC Ensembl
Innerchr2:41107020..41214191hg19UCSC Ensembl
Innerchr2:40960524..41067695hg18UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg38107172
hg19107172
hg18107172
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv581519
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)nssv906903
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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