A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17733745



Internal ID157411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:64260625..64334100hg38UCSC Ensembl
chr20:62891978..62965453hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3873476
hg1973476
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6146992
Supporting Variants
Samples
Known GenesLINC00266-1, PCMTD2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17733745
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.071571


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