A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18022370



Internal ID20589410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:86919931..87008882hg38UCSC Ensembl
chr14:87386275..87475226hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3888952
hg1988952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6495249
Supporting Variants
Samples
Known GenesLOC283585
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18022370
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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