A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17699581



Internal ID123247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:26968298..26968609hg38UCSC Ensembl
chr15:27213445..27213756hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5511213
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17699581
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.030909


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