A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6147022



Internal ID346228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12342928..12343067hg38UCSC Ensembl
chr19:12453742..12453881hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38140
hg19140
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17721491
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6147022
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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