A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519831



Internal ID20893192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32957101..32969000hg38UCSC Ensembl
chr20:31544907..31556806hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg3811900
hg1911900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067423
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519831
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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