A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18217431



Internal ID20784471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:116401331..116419882hg38UCSC Ensembl
chr10:118160843..118179394hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3818552
hg1918552
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6575922
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18217431
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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