A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585622



Internal ID20958693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:21216023..24989723hg38UCSC Ensembl
chr13:21790162..25563861hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg383773701
hg193773700
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223334
Samples
Known GenesANKRD20A19P, ATP12A, BASP1P1, C1QTNF9, C1QTNF9B, C1QTNF9B-AS1, CENPJ, FGF9, LINC00327, LINC00424, LINC00539, LINC00540, MICU2, MIPEP, MIPEPP3, MIR2276, PARP4, RNF17, SACS, SACS-AS1, SGCG, SPATA13, SPATA13-AS1, TNFRSF19, TPTE2P1, TPTE2P6, ZDHHC20
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585622
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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