A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553140



Internal ID20926249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:44654175..44669190hg38UCSC Ensembl
chr20:43282816..43297831hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3815016
hg1915016
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067835
Samples
Known GenesLOC79015
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553140
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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