A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6145397



Internal ID344602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78126272..78145431hg38UCSC Ensembl
chr15:78418614..78437773hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3819160
hg1919160
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17702176
Samples
Known GenesCIB2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6145397
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer