A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6053340



Internal ID21962573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:40117178..40119395hg38UCSC Ensembl
chr19:40623085..40625302hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg382218
hg192218
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17635860
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6053340
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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