A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6385529



Internal ID21043082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:1903357..2070741hg38UCSC Ensembl
chr5:1903471..2070855hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38167385
hg19167385
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215215
Samples
Known GenesMIR548BA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6385529
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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