A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv904507



Internal ID16198463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:24491300..24492157hg38UCSC Ensembl
Innerchr2:24714169..24715026hg19UCSC Ensembl
Innerchr2:24567673..24568530hg18UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38858
hg19858
hg18858
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv581197
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv904507
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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