A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv906868



Internal ID16200824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:38151968..38177244hg38UCSC Ensembl
Innerchr2:38379110..38404386hg19UCSC Ensembl
Innerchr2:38232614..38257890hg18UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg3825277
hg1925277
hg1825277
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv581479
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)nssv906868
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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