A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6402128



Internal ID21059681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13710401..13713400hg38UCSC Ensembl
chr6:13710633..13713632hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg383000
hg193000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216846
Samples
Known GenesRANBP9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6402128
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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