A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581056



Internal ID20954127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:32847966..32848721hg38UCSC Ensembl
chr13:33422104..33422859hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg38756
hg19756
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217502
Samples
Known GenesLINC00423
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581056
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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