A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578040



Internal ID20951111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:96798276..96799549hg38UCSC Ensembl
chr10:98558033..98559306hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg381274
hg191274
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219597
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578040
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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