A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17700074



Internal ID123740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:28106000..28196874hg38UCSC Ensembl
chr15:28351146..28442020hg19UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg3890875
hg1990875
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5500152
Supporting Variants
Samples
Known GenesHERC2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17700074
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000937


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