A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17702590



Internal ID126256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:83486198..83627468hg38UCSC Ensembl
chr15:84154950..84296220hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38141271
hg19141271
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5531801
Supporting Variants
Samples
Known GenesSH3GL3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17702590
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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