A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6140912



Internal ID340106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:177875162..177883324hg38UCSC Ensembl
chr5:177302163..177310325hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg388163
hg198163
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16977679
Samples
Known GenesLOC728554
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6140912
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