A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6328834



Internal ID20861984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:245374130..246219472hg38UCSC Ensembl
chr1:245537432..246382774hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg38845343
hg19845343
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200677
Samples
Known GenesKIF26B, SMYD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6328834
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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