A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv906866



Internal ID16200822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:38117986..38150263hg38UCSC Ensembl
Innerchr2:38345128..38377405hg19UCSC Ensembl
Innerchr2:38198632..38230909hg18UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg3832278
hg1932278
hg1832278
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv581477
Supporting Variants
Samples
Known GenesCYP1B1-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv906866
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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