A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18018014



Internal ID20585054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:37271601..37272400hg38UCSC Ensembl
chr14:37740806..37741605hg19UCSC Ensembl
Cytoband14q13.3
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6490723
Supporting Variants
Samples
Known GenesMIPOL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18018014
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00101


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