A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17701468



Internal ID125134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:37101944..37102031hg38UCSC Ensembl
chr15:37394145..37394232hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5513670
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17701468
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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