A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6144431



Internal ID343636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84489533..84508625hg38UCSC Ensembl
chr15:85034474..85051856hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3819093
hg1917383
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17703567
Samples
Known GenesDNM1P41, GOLGA6L5P
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6144431
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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