A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156339



Internal ID15880405
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
SamplesNINDS_206
Known GenesMSR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156339
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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