A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6387558



Internal ID21045111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:44208099..44242843hg38UCSC Ensembl
chr4:44210116..44244860hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg3834745
hg1934745
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213670
Samples
Known GenesKCTD8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6387558
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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