A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18224306



Internal ID20791346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:112806586..112807583hg38UCSC Ensembl
chr10:114566345..114567342hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg38998
hg19998
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6591560
Supporting Variants
Samples
Known GenesVTI1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18224306
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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