A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18238386



Internal ID20805426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:96048038..96048635hg38UCSC Ensembl
chr14:96514375..96514972hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38598
hg19598
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6582782
Supporting Variants
Samples
Known GenesC14orf132
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18238386
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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