A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv598660



Internal ID16386069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:75052914..75053440hg38UCSC Ensembl
Innerchr5:74348739..74349265hg19UCSC Ensembl
Innerchr5:74384495..74385021hg18UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg38527
hg19527
hg18527
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9879n54
Supporting Variantsnssv1035116, nssv1035117
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv598660
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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