A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18016443



Internal ID20583483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:100104331..100104880hg38UCSC Ensembl
chr14:100570668..100571217hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38550
hg19550
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6502855
Supporting Variants
Samples
Known GenesEVL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18016443
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00042


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