A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156589



Internal ID15876706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:11534141..11571638hg38UCSC Ensembl
Innerchr8:11391650..11429147hg19UCSC Ensembl
Innerchr8:11429059..11466556hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3837498
hg1937498
hg1837498
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv610289
Supporting Variants
SamplesHGDP00883
Known GenesBLK
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156589
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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