A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv598784



Internal ID16039507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:83442024..83480087hg38UCSC Ensembl
Innerchr5:82737843..82775906hg19UCSC Ensembl
Innerchr5:82773599..82811662hg18UCSC Ensembl
Cytoband5q14.2
Allele length
AssemblyAllele length
hg3838064
hg1938064
hg1838064
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1035429
Samples
Known GenesVCAN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv598784
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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