A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1125695



Internal ID15978881
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 StatusS
Merged Variantsnsv612873
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)nssv1125695
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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