A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6371777



Internal ID21029330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:139004622..139008492hg38UCSC Ensembl
chr3:138723464..138727334hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg383871
hg193871
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18093918
Samples
Known GenesPRR23A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6371777
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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