A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18225038



Internal ID20792078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:75151699..75152468hg38UCSC Ensembl
chr10:76911457..76912226hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38770
hg19770
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6582385
Supporting Variants
Samples
Known GenesSAMD8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18225038
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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