A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17702623



Internal ID126289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84165337..84174937hg38UCSC Ensembl
chr15:84834089..84843689hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg389601
hg199601
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6146154
Supporting Variants
Samples
Known GenesLOC100505679
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17702623
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.043478


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