A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18018011



Internal ID20585051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:37197501..37198200hg38UCSC Ensembl
chr14:37666706..37667405hg19UCSC Ensembl
Cytoband14q13.3
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6480931
Supporting Variants
Samples
Known GenesMIPOL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18018011
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.05327


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