A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590530



Internal ID20963601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:96303860..96304713hg38UCSC Ensembl
chr13:96956114..96956967hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38854
hg19854
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231325
Samples
Known GenesHS6ST3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590530
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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