A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv906964



Internal ID16200920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:41003158..41028402hg38UCSC Ensembl
Innerchr2:41230298..41255542hg19UCSC Ensembl
Innerchr2:41083802..41109046hg18UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg3825245
hg1925245
hg1825245
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv581547
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)nssv906964
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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