A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18068908



Internal ID20635948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:3951077..3953198hg38UCSC Ensembl
chr20:3931724..3933845hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg382122
hg192122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6530679
Supporting Variants
Samples
Known GenesRNF24
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18068908
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00015


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