A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535868



Internal ID20909222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62028170..62030612hg38UCSC Ensembl
chr20:60603226..60605668hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg382443
hg192443
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18068318
Samples
Known GenesTAF4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535868
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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