A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17700118



Internal ID123784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40422779..40422817hg38UCSC Ensembl
chr15:40714978..40715016hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38182
hg19182
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5533978
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17700118
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.353887


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