A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18238609



Internal ID20805649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:71633187..71634494hg38UCSC Ensembl
chr14:72099904..72101211hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg381308
hg191308
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6582942
Supporting Variants
Samples
Known GenesSIPA1L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18238609
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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