A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17701097



Internal ID124763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41197834..41197834hg38UCSC Ensembl
chr15:41490032..41490032hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5538474
Supporting Variants
Samples
Known GenesEXD1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17701097
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.012613


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