A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17702926



Internal ID126592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:67508693..67508728hg38UCSC Ensembl
chr15:67801031..67801066hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38285
hg19285
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5548409
Supporting Variants
Samples
Known GenesIQCH-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17702926
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001405


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