A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17702186



Internal ID125852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78328736..78328736hg38UCSC Ensembl
chr15:78621078..78621078hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5535421
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17702186
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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