A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515766



Internal ID20889127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:19275999..19279269hg38UCSC Ensembl
chr20:19256643..19259913hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg383271
hg193271
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18066989
Samples
Known GenesLOC100130264, SLC24A3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515766
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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