A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18247299



Internal ID20814339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:109360170..109360519hg38UCSC Ensembl
chr1:109902792..109903141hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg38350
hg19350
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6537326
Supporting Variants
Samples
Known GenesSORT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18247299
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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