A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373033



Internal ID21030586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:46180413..46182253hg38UCSC Ensembl
chr3:46221905..46223745hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg381841
hg191841
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100684
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373033
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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