A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6057747



Internal ID21966980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:46134388..46240987hg38UCSC Ensembl
chr19:46637645..46744244hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38106600
hg19106600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17619084
Samples
Known GenesDKFZp434J0226, IGFL1, IGFL2, RNU6-66P
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6057747
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