A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6145371



Internal ID344576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:32388000..32394874hg38UCSC Ensembl
chr15:32680201..32687075hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg386875
hg196875
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17701841
Samples
Known GenesGOLGA8K
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6145371
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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