A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18238372



Internal ID20805412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:94411987..94637697hg38UCSC Ensembl
chr14:94878324..95104034hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg38225711
hg19225711
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6591472
Supporting Variants
Samples
Known GenesSERPINA11, SERPINA12, SERPINA3, SERPINA4, SERPINA5, SERPINA9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18238372
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.0001


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