A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6380679



Internal ID21038232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:43338984..43343943hg38UCSC Ensembl
chr4:43341001..43345960hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg384960
hg194960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18116495
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6380679
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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