A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590034



Internal ID20963105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:45867520..45869958hg38UCSC Ensembl
chr12:46261303..46263741hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg382439
hg192439
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232195
Samples
Known GenesARID2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590034
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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