A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593203



Internal ID20966274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97294308..97297641hg38UCSC Ensembl
chr10:99054065..99057398hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg383334
hg193334
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225361
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593203
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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