A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588288



Internal ID20961359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:98166249..98166616hg38UCSC Ensembl
chr10:99926006..99926373hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38368
hg19368
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232453
Samples
Known GenesR3HCC1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588288
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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