A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18093118



Internal ID20660158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:112945238..112949032hg38UCSC Ensembl
chr3:112664085..112667879hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg383795
hg193795
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6369815
Supporting Variants
Samples
Known GenesCD200R1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18093118
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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