A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv598016



Internal ID16385425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:46199293..46399172hg38UCSC Ensembl
Innerchr5:46199395..46399274hg19UCSC Ensembl
Innerchr5:46235152..46435031hg18UCSC Ensembl
Cytoband5p11
Allele length
AssemblyAllele length
hg38199880
hg19199880
hg18199880
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1029710
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv598016
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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