A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv906972



Internal ID16200928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:41003158..41128212hg38UCSC Ensembl
Innerchr2:41230298..41355352hg19UCSC Ensembl
Innerchr2:41083802..41208856hg18UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg38125055
hg19125055
hg18125055
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv581551
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)nssv906972
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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