A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv598937



Internal ID16386346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:91979496..92086065hg38UCSC Ensembl
Innerchr5:91275313..91381882hg19UCSC Ensembl
Innerchr5:91311069..91417638hg18UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38106570
hg19106570
hg18106570
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1038085, nssv1038086
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv598937
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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