A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18068125



Internal ID20635165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:51550440..51551831hg38UCSC Ensembl
chr20:50166979..50168370hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg381392
hg191392
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6552524
Supporting Variants
Samples
Known GenesNFATC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18068125
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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