A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18230151



Internal ID20797191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15593843..15594569hg38UCSC Ensembl
chr10:15635842..15636568hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38727
hg19727
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6590823
Supporting Variants
Samples
Known GenesITGA8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18230151
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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