A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332591



Internal ID20865764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:19879880..19887349hg38UCSC Ensembl
chr1:20206373..20213842hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg387470
hg197470
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202326
Samples
Known GenesOTUD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332591
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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