A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366145



Internal ID21023698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:189129801..189133600hg38UCSC Ensembl
chr3:188847590..188851389hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg383800
hg193800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100294
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366145
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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