A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581645



Internal ID16369054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:42866627..42913513hg38UCSC Ensembl
Innerchr2:43093767..43140653hg19UCSC Ensembl
Innerchr2:42947271..42994157hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3846887
hg1946887
hg1846887
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv907882
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581645
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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