A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589609



Internal ID20962680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:121728050..121728509hg38UCSC Ensembl
chr12:122165956..122166415hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg38460
hg19460
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219070
Samples
Known GenesTMEM120B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589609
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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