A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17699990



Internal ID123656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25097705..25099442hg38UCSC Ensembl
chr15:25342852..25344589hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg381738
hg191738
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5495182
Supporting Variants
Samples
Known GenesSNORD116-25
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17699990
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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