A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18094351



Internal ID20661391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:142535414..142535822hg38UCSC Ensembl
chr3:142254256..142254664hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38409
hg19409
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6356848
Supporting Variants
Samples
Known GenesATR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18094351
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0008


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