A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6393500



Internal ID21051053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:108515873..108543922hg38UCSC Ensembl
chr4:109437029..109465078hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3828050
hg1928050
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209507
Samples
Known GenesRPL34-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6393500
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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