A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18067495



Internal ID20634535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:42523432..42765338hg38UCSC Ensembl
chr20:41152072..41393978hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg38241907
hg19241907
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6549345
Supporting Variants
Samples
Known GenesPTPRT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18067495
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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