A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18228483



Internal ID20795523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:87598553..87599291hg38UCSC Ensembl
chr10:89358310..89359048hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38739
hg19739
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6575789
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18228483
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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