A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5997185



Internal ID21906528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:38797549..38827145hg38UCSC Ensembl
chr4:38799170..38828766hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3829597
hg1929597
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17547412
Samples
Known GenesTLR1, TLR6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5997185
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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