A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18227158



Internal ID20794198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:35026727..35027319hg38UCSC Ensembl
chr14:35495933..35496525hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg38593
hg19593
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6591442
Supporting Variants
Samples
Known GenesSRP54
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18227158
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00061


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