A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17000386



Internal ID67839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:93928130..93928167hg38UCSC Ensembl
chr7:93557442..93557479hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38335
hg19335
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5545390
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17000386
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.013737


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