A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586461



Internal ID20959532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:40919474..40920234hg38UCSC Ensembl
chr13:41493610..41494370hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38761
hg19761
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226659
Samples
Known GenesSUGT1P3, TPTE2P5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586461
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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