A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516403



Internal ID20889764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:20475201..20476600hg38UCSC Ensembl
chr20:20455845..20457244hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067043
Samples
Known GenesRALGAPA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516403
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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