A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6357833



Internal ID21015386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:23434553..23447789hg38UCSC Ensembl
chr3:23476044..23489280hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3813237
hg1913237
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100369
Samples
Known GenesMIR548AC, UBE2E2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6357833
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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