A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18229752



Internal ID20796792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:49554842..49555775hg38UCSC Ensembl
chr14:50021560..50022493hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg38934
hg19934
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6581999
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18229752
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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