A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581286



Internal ID16022009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:32744049..32770756hg38UCSC Ensembl
Innerchr2:32969116..32995823hg19UCSC Ensembl
Innerchr2:32822620..32849327hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg3826708
hg1926708
hg1826708
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv904643
Samples
Known GenesTTC27
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581286
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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