A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18238412



Internal ID20805452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:98736673..98889751hg38UCSC Ensembl
chr14:99203010..99356088hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38153079
hg19153079
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6583423
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18238412
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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