A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18224043



Internal ID20791083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91430831..91751754hg38UCSC Ensembl
chr10:93190588..93511511hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg38320924
hg19320924
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6593400
Supporting Variants
Samples
Known GenesHECTD2, LOC100188947, PPP1R3C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18224043
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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