A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553300



Internal ID20926409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:42586926..42762814hg38UCSC Ensembl
chr20:41215566..41391454hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg38175889
hg19175889
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4463n223
Supporting Variantsnssv18067716
Samples
Known GenesPTPRT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553300
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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