A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6144122



Internal ID343325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:100078979..100088000hg38UCSC Ensembl
chr13:100731233..100740254hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg389022
hg199022
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17692623
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6144122
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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