A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18233204



Internal ID20800244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:50491702..50492593hg38UCSC Ensembl
chr14:50958420..50959311hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg38892
hg19892
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6584743
Supporting Variants
Samples
Known GenesMAP4K5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18233204
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00029


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