A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17703693



Internal ID127359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92511623..92517329hg38UCSC Ensembl
chr15:93054853..93060559hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg385707
hg195707
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5518808
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17703693
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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