A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6333828



Internal ID20867009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:46281948..46318675hg38UCSC Ensembl
chr1:46747620..46784347hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg3836728
hg1936728
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201381
Samples
Known GenesLRRC41, UQCRH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6333828
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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