A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581606



Internal ID16369015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:41816305..41854716hg38UCSC Ensembl
Innerchr2:42043445..42081856hg19UCSC Ensembl
Innerchr2:41896949..41935360hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3838412
hg1938412
hg1838412
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv907421
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581606
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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