A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18247309



Internal ID20814349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:109724411..109724649hg38UCSC Ensembl
chr1:110267033..110267271hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg38239
hg19239
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6537273
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18247309
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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