A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv906850



Internal ID16200806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:35961047..36104655hg38UCSC Ensembl
Innerchr2:36186152..36331798hg19UCSC Ensembl
Innerchr2:36039656..36185302hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38143609
hg19145647
hg18145647
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv581460
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)nssv906850
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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