A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541029



Internal ID20914314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:42892244..43071383hg38UCSC Ensembl
chr20:41520884..41700023hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg38179140
hg19179140
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202863
Samples
Known GenesPTPRT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541029
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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