A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6389251



Internal ID21046804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:61955001..62091800hg38UCSC Ensembl
chr4:62820719..62957518hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg38136800
hg19136800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5280n223
Supporting Variantsnssv18210908
Samples
Known GenesLPHN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6389251
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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