A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6410879



Internal ID21068432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:113587901..113611400hg38UCSC Ensembl
chr5:112923598..112947097hg19UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg3823500
hg1923500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212438
Samples
Known GenesYTHDC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6410879
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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