A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596901



Internal ID16384310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:2041551..2066051hg38UCSC Ensembl
Innerchr5:2041665..2066165hg19UCSC Ensembl
Innerchr5:2094665..2119165hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3824501
hg1924501
hg1824501
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9544n54
Supporting Variantsnssv1023651, nssv1023652
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596901
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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