A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593859



Internal ID20966930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:22904574..24978653hg38UCSC Ensembl
chr13:23478713..25552791hg19UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg382074080
hg192074079
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233836
Samples
Known GenesANKRD20A19P, ATP12A, C1QTNF9, C1QTNF9B, C1QTNF9B-AS1, CENPJ, LINC00327, MIPEP, MIR2276, PARP4, RNF17, SACS, SACS-AS1, SGCG, SPATA13, SPATA13-AS1, TNFRSF19, TPTE2P1, TPTE2P6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593859
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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