A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231377



Internal ID20798417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:34360195..34395591hg38UCSC Ensembl
chr6:34327972..34363368hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3835397
hg1935397
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6404033
Supporting Variants
Samples
Known GenesNUDT3, RPS10-NUDT3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231377
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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