A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17699775



Internal ID123441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42324212..42324509hg38UCSC Ensembl
chr15:42616410..42616707hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38298
hg19298
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5509423
Supporting Variants
Samples
Known GenesGANC
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17699775
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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