A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6018203



Internal ID21927546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:161377273..161404564hg38UCSC Ensembl
chr5:160804279..160831570hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3827292
hg1927292
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17561959
Samples
Known GenesGABRB2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6018203
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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