A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373163



Internal ID21030716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:341355..566560hg38UCSC Ensembl
chr4:335144..560349hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38225206
hg19225206
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212915
Samples
Known GenesABCA11P, PIGG, ZNF141, ZNF721
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373163
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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