A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18018051



Internal ID20585091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:37519163..37519627hg38UCSC Ensembl
chr14:37988368..37988832hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38465
hg19465
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6495229
Supporting Variants
Samples
Known GenesMIPOL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18018051
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0008


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