A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18238382



Internal ID20805422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:95392901..95433070hg38UCSC Ensembl
chr14:95859238..95899407hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg3840170
hg1940170
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6576769
Supporting Variants
Samples
Known GenesLINC00341, SYNE3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18238382
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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