A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536635



Internal ID20909980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:45537100..45547663hg38UCSC Ensembl
chr20:44165739..44176302hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3810564
hg1910564
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18068342
Samples
Known GenesEPPIN, EPPIN-WFDC6, WFDC6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536635
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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