A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4740541



Internal ID20516517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:57064646..57072050hg38UCSC Ensembl
chr18:54731877..54739281hg19UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg387405
hg197405
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16275572
Samples
Known GenesLINC-ROR
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4740541
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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