A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6611053



Internal ID20984124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:137036982..137080271hg38UCSC Ensembl
chr6:137358119..137401408hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3843290
hg1943290
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216842
Samples
Known GenesIL20RA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6611053
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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