A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18221496



Internal ID20788536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:49913245..49914114hg38UCSC Ensembl
chr14:50379963..50380832hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg38870
hg19870
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6581042
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18221496
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00018


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