A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594066



Internal ID20967137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:100202167..100202774hg38UCSC Ensembl
chr14:100668504..100669111hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38608
hg19608
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235749
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594066
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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