A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540665



Internal ID20913954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:42549793..42621071hg38UCSC Ensembl
chr20:41178433..41249711hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg3871279
hg1971279
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4464n223
Supporting Variantsnssv18067500
Samples
Known GenesPTPRT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540665
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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