A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533725



Internal ID20907086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:25683689..25684395hg38UCSC Ensembl
chr20:25664325..25665031hg19UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg38707
hg19707
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067184
Samples
Known GenesZNF337
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533725
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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