A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv598149



Internal ID16385558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:51981695..52131895hg38UCSC Ensembl
Innerchr5:51277529..51427729hg19UCSC Ensembl
Innerchr5:51313286..51463486hg18UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38150201
hg19150201
hg18150201
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9782n54
Supporting Variantsnssv1153931
Samples1782681169_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv598149
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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