A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6145726



Internal ID344931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16069363..16069756hg38UCSC Ensembl
chr19:16180173..16180566hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38394
hg19394
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17721835
Samples
Known GenesTPM4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6145726
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