A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18018343



Internal ID20585383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:43220960..44533842hg38UCSC Ensembl
chr14:43690163..45003045hg19UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg381312883
hg191312883
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6483668
Supporting Variants
Samples
Known GenesFSCB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18018343
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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