A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17699771



Internal ID123437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42286114..42329049hg38UCSC Ensembl
chr15:42578312..42621247hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3842936
hg1942936
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5509147
Supporting Variants
Samples
Known GenesGANC
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17699771
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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