A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17704066



Internal ID127732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:82340874..82360400hg38UCSC Ensembl
chr15:82633228..83029123hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3819527
hg19395896
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6145704
Supporting Variants
Samples
Known GenesADAMTS7P1, CSPG4P8, GOLGA6L10, GOLGA6L20, GOLGA6L9, LOC727751, LOC80154, RPS17, RPS17L, UBE2Q2P2, UBE2Q2P3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17704066
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.182678


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