A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17700083



Internal ID123749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:39519562..39519562hg38UCSC Ensembl
chr15:39811763..39811763hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5424960
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17700083
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.070774


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