A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156338



Internal ID15879608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:16092262..16171585hg38UCSC Ensembl
Innerchr8:15949771..16029094hg19UCSC Ensembl
Innerchr8:15994142..16073465hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3879324
hg1979324
hg1879324
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv610589
Supporting Variants
SamplesHGDP01402
Known GenesMSR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156338
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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