A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581646



Internal ID16369055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:42916447..42928842hg38UCSC Ensembl
Innerchr2:43143587..43155982hg19UCSC Ensembl
Innerchr2:42997091..43009486hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3812396
hg1912396
hg1812396
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv907883
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581646
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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