A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18068079



Internal ID20635119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36888539..36893416hg38UCSC Ensembl
chr20:35516942..35521819hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg384878
hg194878
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6534272
Supporting Variants
Samples
Known GenesSAMHD1, TLDC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18068079
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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