A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6397343



Internal ID21054896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:113571122..113611404hg38UCSC Ensembl
chr5:112906819..112947101hg19UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg3840283
hg1940283
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212437
Samples
Known GenesYTHDC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6397343
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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