A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178946



Internal ID20745986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:87761238..87784279hg38UCSC Ensembl
chr14:88227582..88250623hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3823042
hg1923042
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6485845
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178946
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00026


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