A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413217



Internal ID21070770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:64442546..64458893hg38UCSC Ensembl
chr6:65152439..65168786hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3816348
hg1916348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18143566
Samples
Known GenesEYS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413217
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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