A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18100514



Internal ID20667554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:189285901..189287500hg38UCSC Ensembl
chr3:189003690..189005289hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6373741
Supporting Variants
Samples
Known GenesTPRG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18100514
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00651


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