A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1106961



Internal ID15960147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:16090726..16162448hg38UCSC Ensembl
Innerchr8:15948235..16019957hg19UCSC Ensembl
Innerchr8:15992606..16064328hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3871723
hg1971723
hg1871723
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv610582
Supporting Variants
Samples
Known GenesMSR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1106961
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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