A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18247293



Internal ID20814333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:109076878..109077190hg38UCSC Ensembl
chr1:109619500..109619812hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6552170
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18247293
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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