A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18225617



Internal ID20792657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:49628943..49630183hg38UCSC Ensembl
chr14:50095661..50096901hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg381241
hg191241
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6586889
Supporting Variants
Samples
Known GenesDNAAF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18225617
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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