A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226684



Internal ID20793724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:807000..1147957hg38UCSC Ensembl
chr10:852940..1193897hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38340958
hg19340958
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6576935
Supporting Variants
Samples
Known GenesGTPBP4, IDI1, IDI2, IDI2-AS1, LARP4B, WDR37
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18226684
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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