A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6055703



Internal ID21964936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:40248874..40248945hg38UCSC Ensembl
chr19:40754781..40754852hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17622779
Samples
Known GenesAKT2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6055703
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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