A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18017972



Internal ID20585012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:36639838..36640388hg38UCSC Ensembl
chr14:37109043..37109593hg19UCSC Ensembl
Cytoband14q13.3
Allele length
AssemblyAllele length
hg38551
hg19551
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6476786
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18017972
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00064


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