A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223967



Internal ID20791007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:36704372..36705345hg38UCSC Ensembl
chr14:37173577..37174550hg19UCSC Ensembl
Cytoband14q13.3
Allele length
AssemblyAllele length
hg38974
hg19974
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6591555
Supporting Variants
Samples
Known GenesSLC25A21
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223967
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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