A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6357487



Internal ID21015040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:179716855..179718537hg38UCSC Ensembl
chr3:179434643..179436325hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg381683
hg191683
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18099799
Samples
Known GenesUSP13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6357487
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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