A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589970



Internal ID16377379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:26383758..26396620hg38UCSC Ensembl
Innerchr3:26425249..26438111hg19UCSC Ensembl
Innerchr3:26400253..26413115hg18UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3812863
hg1912863
hg1812863
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8266n54
Supporting Variantsnssv960150, nssv960151, nssv960149, nssv960154, nssv960153, nssv960152, nssv960148
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589970
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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