A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18225165



Internal ID20792205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23001538..23002067hg38UCSC Ensembl
chr14:23470747..23471276hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38530
hg19530
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6584982
Supporting Variants
Samples
Known GenesC14orf93
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18225165
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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