A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18217774



Internal ID20784814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:52679721..52680098hg38UCSC Ensembl
chr14:53146439..53146816hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg38378
hg19378
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6582397
Supporting Variants
Samples
Known GenesERO1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18217774
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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