A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597370



Internal ID16038093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:18092115..18723359hg38UCSC Ensembl
Innerchr5:18092224..18723468hg19UCSC Ensembl
Innerchr5:18127981..18759225hg18UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg38631245
hg19631245
hg18631245
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1026409
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597370
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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