A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv600167



Internal ID16040890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:160806749..160863163hg38UCSC Ensembl
Innerchr5:160233756..160290170hg19UCSC Ensembl
Innerchr5:160166334..160222748hg18UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3856415
hg1956415
hg1856415
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1044635
Samples
Known GenesATP10B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv600167
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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