A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17623182



Internal ID21815229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:50946270..50946503hg38UCSC Ensembl
chr18:48472640..48472873hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg38234
hg19234
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6023505
Supporting Variants
Samples
Known GenesME2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17623182
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