A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219949



Internal ID20786989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:49644060..49644544hg38UCSC Ensembl
chr14:50110778..50111262hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg38485
hg19485
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6594427
Supporting Variants
Samples
Known GenesPOLE2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219949
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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