A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325486



Internal ID20858617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:22286759..22470864hg38UCSC Ensembl
chr1:22613252..22797357hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg38184106
hg19184106
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202065
Samples
Known GenesZBTB40
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325486
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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