A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219291



Internal ID20786331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73202075..73202495hg38UCSC Ensembl
chr10:74961833..74962253hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38421
hg19421
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6579668
Supporting Variants
Samples
Known GenesFAM149B1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219291
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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