A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6534641



Internal ID20908002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:19219959..19222109hg38UCSC Ensembl
chr20:19200603..19202753hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg382151
hg192151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18066985
Samples
Known GenesSLC24A3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6534641
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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