A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17704068



Internal ID127734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:82340874..82347874hg38UCSC Ensembl
chr15:82633228..83016597hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg387001
hg19383370
Variant TypeOTHER copy number variation
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5429913
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)nssv17704068
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.438272


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