A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6045827



Internal ID21955085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:34321050..34321227hg38UCSC Ensembl
chr19:34811955..34812132hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38178
hg19178
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17626621
Samples
Known GenesKIAA0355
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6045827
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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