A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1109440



Internal ID15962626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:29980105..29991150hg38UCSC Ensembl
Innerchr8:29837621..29848666hg19UCSC Ensembl
Innerchr8:29957163..29968208hg18UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3811046
hg1911046
hg1811046
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv610874
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)nssv1109440
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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