A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4731668



Internal ID20507588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:56600364..56600431hg38UCSC Ensembl
chr18:54267595..54267662hg19UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16262408
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4731668
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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