A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv599292



Internal ID16386701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:106300124..106492488hg38UCSC Ensembl
Innerchr5:105635825..105828189hg19UCSC Ensembl
Innerchr5:105663724..105856088hg18UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg38192365
hg19192365
hg18192365
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1039773
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv599292
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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