A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156841



Internal ID15507203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:55810132..55961458hg38UCSC Ensembl
Innerchr8:56722691..56874017hg19UCSC Ensembl
Innerchr8:56885245..57036571hg18UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38151327
hg19151327
hg18151327
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv611397
Supporting Variants
Samples1780854477_A
Known GenesLYN, TGS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156841
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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