A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581943



Internal ID20955014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:25014412..26066804hg38UCSC Ensembl
chr13:25588550..26640942hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg381052393
hg191052393
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1782n223
Supporting Variantsnssv18232647
Samples
Known GenesAMER2, ATP8A2, MTMR6, NUPL1, PABPC3, SHISA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581943
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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