A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18068352



Internal ID20635392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:45701912..45702535hg38UCSC Ensembl
chr20:44330551..44331174hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38624
hg19624
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6553076
Supporting Variants
Samples
Known GenesWFDC10B, WFDC13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18068352
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00039


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