A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366511



Internal ID21024064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:112935043..112940395hg38UCSC Ensembl
chr3:112653890..112659242hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg385353
hg195353
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18093115
Samples
Known GenesCD200R1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366511
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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