A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580196



Internal ID20953267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:1743324..1744103hg38UCSC Ensembl
chr12:1852490..1853269hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg38780
hg19780
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225207
Samples
Known GenesADIPOR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580196
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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