A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517110



Internal ID20890471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:20498176..20502553hg38UCSC Ensembl
chr20:20478820..20483197hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg384378
hg194378
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067044
Samples
Known GenesRALGAPA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517110
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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