A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18143343



Internal ID20710383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:41868452..41868888hg38UCSC Ensembl
chr6:41836190..41836626hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38437
hg19437
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6405720
Supporting Variants
Samples
Known GenesUSP49
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18143343
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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