A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406303



Internal ID21063856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:46404101..46410600hg38UCSC Ensembl
chr6:46371838..46378337hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg386500
hg196500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233654
Samples
Known GenesRCAN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406303
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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