A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18179961



Internal ID20747001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:88619494..88619954hg38UCSC Ensembl
chr14:89085838..89086298hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg38461
hg19461
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6512990
Supporting Variants
Samples
Known GenesEML5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18179961
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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