A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612873



Internal ID16400282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:143618822..143631764hg38UCSC Ensembl
Innerchr8:144700992..144713934hg19UCSC Ensembl
Innerchr8:144772135..144785077hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3812943
hg1912943
hg1812943
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12427n54
Supporting Variantsnssv1125696, nssv1125695
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612873
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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