A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6404563



Internal ID21062116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35448889..35493573hg38UCSC Ensembl
chr6:35416666..35461350hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3844685
hg1944685
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220030
Samples
Known GenesFANCE, MIR7111, RPL10A, TEAD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6404563
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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