A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583971



Internal ID20957042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:133195761..133196195hg38UCSC Ensembl
chr12:133772347..133772781hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg38435
hg19435
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218774
Samples
Known GenesZNF268
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583971
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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