A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6046550



Internal ID21955789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44500676..44507633hg38UCSC Ensembl
chr19:45004728..45011685hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg386958
hg196958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17628507
Samples
Known GenesCEACAM20
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6046550
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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