A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18237180



Internal ID20804220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:61678635..61680228hg38UCSC Ensembl
chr14:62145353..62146946hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg381594
hg191594
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6580815
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18237180
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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