A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6612323



Internal ID20985394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:127256701..127272300hg38UCSC Ensembl
chr6:127577846..127593445hg19UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg3815600
hg1915600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215519
Samples
Known GenesRNF146
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6612323
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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