A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6389808



Internal ID21047361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:135902241..136257806hg38UCSC Ensembl
chr4:136823396..137178961hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38355566
hg19355566
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210840
Samples
Known GenesLINC00613
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6389808
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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