A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6393686



Internal ID21051239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:18823781..18950911hg38UCSC Ensembl
chr5:18823890..18951020hg19UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg38127131
hg19127131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5686n223
Supporting Variantsnssv18129045
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6393686
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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