A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv598157



Internal ID16385566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:52045037..52146437hg38UCSC Ensembl
Innerchr5:51340871..51442271hg19UCSC Ensembl
Innerchr5:51376628..51478028hg18UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38101401
hg19101401
hg18101401
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9783n54
Supporting Variantsnssv1030342
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv598157
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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