A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6042534



Internal ID21951850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:8018374..8018510hg38UCSC Ensembl
chr20:7999021..7999157hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17633776
Samples
Known GenesTMX4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6042534
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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