A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220155



Internal ID20787195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102639762..102641165hg38UCSC Ensembl
chr14:103106099..103107502hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg381404
hg191404
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6578341
Supporting Variants
Samples
Known GenesRCOR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220155
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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