A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18022713



Internal ID20589753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:90773357..90774165hg38UCSC Ensembl
chr14:91239701..91240509hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg38809
hg19809
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6503898
Supporting Variants
Samples
Known GenesTTC7B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18022713
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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