A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18228903



Internal ID20795943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73400162..73400890hg38UCSC Ensembl
chr10:75159920..75160648hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38729
hg19729
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6591836
Supporting Variants
Samples
Known GenesANXA7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18228903
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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