A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18249961



Internal ID20817001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:205102054..205102585hg38UCSC Ensembl
chr1:205071182..205071713hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38532
hg19532
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6549670
Supporting Variants
Samples
Known GenesRBBP5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18249961
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00024


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