A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4749989



Internal ID20526024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:68197328..68200214hg38UCSC Ensembl
chr4:69063046..69065932hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg382887
hg192887
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16276630
Samples
Known GenesFTLP10, TMPRSS11BNL
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4749989
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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