A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6022615



Internal ID21931958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:71565505..71567259hg38UCSC Ensembl
chr18:69232741..69234495hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg381755
hg191755
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17634780
Samples
Known GenesLOC100505776
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6022615
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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