A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536968



Internal ID20910312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:58333709..58338044hg38UCSC Ensembl
chr20:56908765..56913100hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg384336
hg194336
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18069112
Samples
Known GenesRAB22A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536968
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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