A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18237307



Internal ID20804347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:75606282..75606695hg38UCSC Ensembl
chr14:76072625..76073038hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38414
hg19414
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6582745
Supporting Variants
Samples
Known GenesFLVCR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18237307
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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