A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553679



Internal ID20926790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:45879601..45885405hg38UCSC Ensembl
chr20:44508240..44514044hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg385805
hg195805
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18068365
Samples
Known GenesZSWIM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553679
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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