A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6384857



Internal ID21042410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:119626801..119629100hg38UCSC Ensembl
chr4:120547956..120550255hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210203
Samples
Known GenesPDE5A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6384857
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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