A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5429913



Internal ID208745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:82340874..82347874hg38UCSC Ensembl
chr15:82633228..83016597hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg387001
hg19383370
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17704068
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)nsv5429913
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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