A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6337353



Internal ID20994906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:46534858..46542789hg38UCSC Ensembl
chr2:46761997..46769928hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg387932
hg197932
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209819
Samples
Known GenesRHOQ
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6337353
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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