A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412876



Internal ID21070429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:64719676..64741493hg38UCSC Ensembl
chr6:65429569..65451386hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3821818
hg1921818
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18145613
Samples
Known GenesEYS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412876
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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