A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6147401



Internal ID346582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45084978..45085123hg38UCSC Ensembl
chr19:45588236..45588381hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38146
hg19146
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17725285
Samples
Known GenesGEMIN7
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6147401
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