A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18018205



Internal ID20585245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:39150663..39153741hg38UCSC Ensembl
chr14:39619867..39622945hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg383079
hg193079
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6485757
Supporting Variants
Samples
Known GenesTRAPPC6B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18018205
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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