A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4738329



Internal ID20514297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:61584064..61584129hg38UCSC Ensembl
chr18:59251297..59251362hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16279866
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4738329
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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