A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582994



Internal ID20956065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:77580460..77581585hg38UCSC Ensembl
chr14:78046803..78047928hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg381126
hg191126
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237533
Samples
Known GenesSPTLC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6582994
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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