A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584622



Internal ID20957693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:14740528..14742197hg38UCSC Ensembl
chr12:14893462..14895131hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg381670
hg191670
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225166
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584622
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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