A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18229286



Internal ID20796326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:96915240..96916203hg38UCSC Ensembl
chr10:98674997..98675960hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg38964
hg19964
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6591992
Supporting Variants
Samples
Known GenesLCOR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18229286
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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