A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587346



Internal ID20960417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110309258..110309908hg38UCSC Ensembl
chr12:110747063..110747713hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38651
hg19651
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1691n223
Supporting Variantsnssv18230359
Samples
Known GenesATP2A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587346
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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