A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6534427



Internal ID20907788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32470315..32471942hg38UCSC Ensembl
chr20:31058118..31059745hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg381628
hg191628
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067390
Samples
Known GenesC20orf112
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6534427
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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