A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6364793



Internal ID21022346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:170084786..170090123hg38UCSC Ensembl
chr3:169802574..169807911hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg385338
hg195338
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18097145
Samples
Known GenesGPR160, PHC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6364793
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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