A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17700835



Internal ID124501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:57350452..57488224hg38UCSC Ensembl
chr15:57642650..57780422hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38137773
hg19137773
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5529922
Supporting Variants
Samples
Known GenesCGNL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17700835
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001405


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