A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611396



Internal ID16052119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:55799154..55963660hg38UCSC Ensembl
Innerchr8:56711713..56876219hg19UCSC Ensembl
Innerchr8:56874267..57038773hg18UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38164507
hg19164507
hg18164507
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12173n54
Supporting Variantsnssv1156840
Samples1780862082_A
Known GenesLYN, TGS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611396
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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