A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6145991



Internal ID345196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:101900533..101970133hg38UCSC Ensembl
chr15:102440736..102510336hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3869601
hg1969601
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17705619
Samples
Known GenesFAM138E, OR4F4, WASH3P
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6145991
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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