A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6144479



Internal ID343684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:32156874..32266874hg38UCSC Ensembl
chr15:32449075..32559075hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38110001
hg19110001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17701821
Samples
Known GenesCHRNA7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6144479
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