A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18021167



Internal ID20588207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:76071813..76073181hg38UCSC Ensembl
chr14:76538156..76539524hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg381369
hg191369
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6478329
Supporting Variants
Samples
Known GenesIFT43
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18021167
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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