A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18068076



Internal ID20635116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36876519..36877079hg38UCSC Ensembl
chr20:35504922..35505482hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38561
hg19561
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6530755
Supporting Variants
Samples
Known GenesTLDC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18068076
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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