A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18021396



Internal ID20588436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:81361845..81367430hg38UCSC Ensembl
chr14:81828189..81833774hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg385586
hg195586
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6494335
Supporting Variants
Samples
Known GenesSTON2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18021396
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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