A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539204



Internal ID20912508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:57504166..57505438hg38UCSC Ensembl
chr20:56079222..56080494hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg381273
hg191273
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18069077
Samples
Known GenesCTCFL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539204
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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