A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611400



Internal ID16398809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:56142495..56186746hg38UCSC Ensembl
Innerchr8:57055054..57099305hg19UCSC Ensembl
Innerchr8:57217608..57261859hg18UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3844252
hg1944252
hg1844252
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12174n54
Supporting Variantsnssv1115585
Samples
Known GenesPLAG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611400
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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