A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18020699



Internal ID20587739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:64523701..64524900hg38UCSC Ensembl
chr14:64990419..64991618hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6485296
Supporting Variants
Samples
Known GenesZBTB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18020699
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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