A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6386928



Internal ID21044481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:114713030..114759872hg38UCSC Ensembl
chr4:115634186..115681028hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg3846843
hg1946843
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18106417
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6386928
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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