A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595379



Internal ID20968450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:24580561..24968592hg38UCSC Ensembl
chr13:25154699..25542730hg19UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg38388032
hg19388032
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1779n223
Supporting Variantsnssv18234753
Samples
Known GenesATP12A, CENPJ, RNF17, TPTE2P1, TPTE2P6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595379
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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