A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6146204



Internal ID345409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41109224..41111300hg38UCSC Ensembl
chr15:41401422..41403498hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg382077
hg192077
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17700162
Samples
Known GenesINO80
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6146204
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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