A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18145613



Internal ID20712653
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 StatusS
Merged Variantsnsv6412876
Supporting Variants
Samples
Known GenesEYS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18145613
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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