A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590381



Internal ID20963452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:36470971..36488156hg38UCSC Ensembl
chr14:36940176..36957361hg19UCSC Ensembl
Cytoband14q13.3
Allele length
AssemblyAllele length
hg3817186
hg1917186
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221213
Samples
Known GenesSFTA3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590381
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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