A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6383304



Internal ID21040857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43018690..43028550hg38UCSC Ensembl
chr5:43018792..43028652hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg389861
hg199861
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18130488
Samples
Known GenesLOC648987
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6383304
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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