A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5538633



Internal ID313696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:56897131..56897165hg38UCSC Ensembl
chr17:54974492..54974526hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38337
hg19337
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17724827
Samples
Known GenesTRIM25
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5538633
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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