A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6054548



Internal ID21963781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36162898..36163220hg38UCSC Ensembl
chr19:36653800..36654122hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17634783
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6054548
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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