A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596902



Internal ID16384311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:2041551..2069095hg38UCSC Ensembl
Innerchr5:2041665..2069209hg19UCSC Ensembl
Innerchr5:2094665..2122209hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3827545
hg1927545
hg1827545
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9544n54
Supporting Variantsnssv1023653
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596902
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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