A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6141958



Internal ID341158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:131414000..131576552hg38UCSC Ensembl
chr9:134289387..134451939hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg38162553
hg19162553
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17029884
Samples
Known GenesPOMT1, PRRC2B, SNORD62A, SNORD62B, UCK1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6141958
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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