A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18235601



Internal ID20802641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:34755865..34758474hg38UCSC Ensembl
chr14:35225071..35227680hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg382610
hg192610
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6589479
Supporting Variants
Samples
Known GenesBAZ1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18235601
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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