A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18020706



Internal ID20587746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:64810390..64815400hg38UCSC Ensembl
chr14:65277108..65282118hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg385011
hg195011
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6477972
Supporting Variants
Samples
Known GenesSPTB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18020706
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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