A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581773



Internal ID16369182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:48050351..48215970hg38UCSC Ensembl
Innerchr2:48277490..48443109hg19UCSC Ensembl
Innerchr2:48130994..48296613hg18UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg38165620
hg19165620
hg18165620
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv908147, nssv908148
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581773
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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