A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18230119



Internal ID20797159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103205613..103520468hg38UCSC Ensembl
chr10:104965370..105280225hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg38314856
hg19314856
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6594978
Supporting Variants
Samples
Known GenesCALHM1, CALHM2, CALHM3, INA, LOC729020, MIR1307, NEURL1, PCGF6, PDCD11, TAF5, USMG5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18230119
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00102


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