A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6109746



Internal ID22018979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:34896137..34896137hg38UCSC Ensembl
chr19:35387041..35387041hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17623914
Samples
Known GenesLINC00904
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6109746
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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