A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6404063



Internal ID21061616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:64221512..64256466hg38UCSC Ensembl
chr6:64931405..64966359hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3834955
hg1934955
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230064
Samples
Known GenesEYS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6404063
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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