A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6411794



Internal ID21069347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29502709..29574025hg38UCSC Ensembl
chr6:29470486..29541802hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3871317
hg1971317
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230512
Samples
Known GenesLINC01015, UBD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6411794
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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