A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6041112



Internal ID21950448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:55338511..55338565hg38UCSC Ensembl
chr19:55849879..55849933hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17625747
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6041112
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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