A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6145899



Internal ID345104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78538345..78538406hg38UCSC Ensembl
chr15:78830687..78830748hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17702196
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6145899
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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