A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5868825



Internal ID22643760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:42824838..42827037hg38UCSC Ensembl
chr20:41453478..41455677hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17486013
Samples
Known GenesPTPRT
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5868825
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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