A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6378412



Internal ID21035965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:33511886..33513271hg38UCSC Ensembl
chr5:33511991..33513376hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg381386
hg191386
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18129675
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6378412
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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