A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539297



Internal ID20912598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:42824080..42835882hg38UCSC Ensembl
chr20:41452720..41464522hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg3811803
hg1911803
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4466n223
Supporting Variantsnssv18067737
Samples
Known GenesPTPRT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539297
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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