A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv599618



Internal ID16387027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:121517974..121575376hg38UCSC Ensembl
Innerchr5:120853669..120911071hg19UCSC Ensembl
Innerchr5:120881568..120938970hg18UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3857403
hg1957403
hg1857403
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1031994
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv599618
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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