A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17703939



Internal ID127605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69077353..69078214hg38UCSC Ensembl
chr15:69369693..69370554hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38862
hg19862
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5520303
Supporting Variants
Samples
Known GenesMIR548H4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17703939
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000937


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