A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6376021



Internal ID21033574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:41754769..41757668hg38UCSC Ensembl
chr5:41754871..41757770hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg382900
hg192900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5736n223
Supporting Variantsnssv18131015
Samples
Known GenesOXCT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6376021
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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