A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6402898



Internal ID21060451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:26427234..26464554hg38UCSC Ensembl
chr6:26427462..26464782hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg3837321
hg1937321
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220752
Samples
Known GenesBTN2A1, BTN2A3P, BTN3A3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6402898
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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