A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405960



Internal ID21063513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:64024686..64032158hg38UCSC Ensembl
chr6:64734579..64742051hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg387473
hg197473
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219273
Samples
Known GenesEYS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405960
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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