A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18233395



Internal ID20800435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:35026917..35027090hg38UCSC Ensembl
chr14:35496123..35496296hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg38174
hg19174
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6591691
Supporting Variants
Samples
Known GenesSRP54
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18233395
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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