A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17703169



Internal ID126835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60529354..60530701hg38UCSC Ensembl
chr15:60821553..60822900hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg381348
hg191348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5514820
Supporting Variants
Samples
Known GenesRORA
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17703169
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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