A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6365342



Internal ID21022895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:126610711..126615081hg38UCSC Ensembl
chr3:126329554..126333924hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg384371
hg194371
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094065
Samples
Known GenesTXNRD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6365342
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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