A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399113



Internal ID21056666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:139400918..139411449hg38UCSC Ensembl
chr5:138736607..138747138hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg3810532
hg1910532
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18125411
Samples
Known GenesDNAJC18, SPATA24
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399113
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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