A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6021991



Internal ID21931334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:39573955..39598610hg38UCSC Ensembl
chr18:37153919..37178574hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3824656
hg1924656
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17620629
Samples
Known GenesLINC00669
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6021991
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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