A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1125699



Internal ID15978885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:143618822..143631836hg38UCSC Ensembl
Innerchr8:144700992..144714006hg19UCSC Ensembl
Innerchr8:144772135..144785149hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3813015
hg1913015
hg1813015
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv612874
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)nssv1125699
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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