A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv598829



Internal ID16386238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:85797753..85902372hg38UCSC Ensembl
Innerchr5:85093571..85198190hg19UCSC Ensembl
Innerchr5:85129327..85233946hg18UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38104620
hg19104620
hg18104620
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9917n54
Supporting Variantsnssv1035777
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv598829
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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