A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18225601



Internal ID20792641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:110018414..110019503hg38UCSC Ensembl
chr10:111778172..111779261hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg381090
hg191090
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6589871
Supporting Variants
Samples
Known GenesADD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18225601
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00012


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