A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551783



Internal ID20924916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:44649984..44653197hg38UCSC Ensembl
chr20:43278625..43281838hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg383214
hg193214
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067834
Samples
Known GenesADA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551783
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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