A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6145404



Internal ID344609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11302891..11304746hg38UCSC Ensembl
chr19:11413567..11415422hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381856
hg191856
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17721396
Samples
Known GenesTSPAN16
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6145404
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