A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17628507



Internal ID21820554
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 StatusS
Merged Variantsnsv6046550
Supporting Variants
Samples
Known GenesCEACAM20
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17628507
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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