A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17702544



Internal ID126210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:82628241..82789039hg38UCSC Ensembl
chr15:83296992..83457791hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38160799
hg19160800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5514636
Supporting Variants
Samples
Known GenesAP3B2, CPEB1, FSD2, LOC283692, LOC283693, LOC338963, SCARNA15
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17702544
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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