A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581262



Internal ID16368671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:30400196..30410930hg38UCSC Ensembl
Innerchr2:30623062..30633796hg19UCSC Ensembl
Innerchr2:30476566..30487300hg18UCSC Ensembl
Cytoband2p23.1
Allele length
AssemblyAllele length
hg3810735
hg1910735
hg1810735
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv904618
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581262
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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