A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18247146



Internal ID20814186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155905846..155906708hg38UCSC Ensembl
chr1:155875637..155876499hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg38863
hg19863
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6552100
Supporting Variants
Samples
Known GenesRIT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18247146
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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