A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580036



Internal ID20953107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:96212860..96217763hg38UCSC Ensembl
chr14:96679197..96684100hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg384904
hg194904
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238388
Samples
Known GenesBDKRB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580036
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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