A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596929



Internal ID16384338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:3848742..3873627hg38UCSC Ensembl
Innerchr5:3848856..3873741hg19UCSC Ensembl
Innerchr5:3901856..3926741hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3824886
hg1924886
hg1824886
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1023685
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596929
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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