A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587424



Internal ID20960495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:98719376..98735252hg38UCSC Ensembl
chr10:100479133..100495009hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg3815877
hg1915877
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232713
Samples
Known GenesHPSE2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587424
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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