A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18067662



Internal ID20634703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:42455383..42455788hg38UCSC Ensembl
chr20:41084023..41084428hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg38406
hg19406
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6536281
Supporting Variants
Samples
Known GenesPTPRT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18067662
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00126


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