A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552066



Internal ID20925196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:58982400..58987692hg38UCSC Ensembl
chr20:57557455..57562747hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg385293
hg195293
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18069133
Samples
Known GenesNELFCD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552066
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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