A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6145694



Internal ID344899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:37304874..37313000hg38UCSC Ensembl
chr15:37597075..37605201hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg388127
hg198127
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17701484
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6145694
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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