A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6550469



Internal ID20923610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:44215752..44243367hg38UCSC Ensembl
chr20:42844392..42872007hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3827616
hg1927616
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067811
Samples
Known GenesOSER1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6550469
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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