A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516804



Internal ID20890165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:20430807..20433713hg38UCSC Ensembl
chr20:20411451..20414357hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg382907
hg192907
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067041
Samples
Known GenesRALGAPA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516804
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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