A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6026364



Internal ID21935707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:23911014..23911157hg38UCSC Ensembl
chr18:21490978..21491121hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17618750
Samples
Known GenesLAMA3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6026364
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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