A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17637486



Internal ID21829533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:41768680..41768809hg38UCSC Ensembl
chr19:42272589..42272718hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6040590
Supporting Variants
Samples
Known GenesCEACAM6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17637486
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer