A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18251159



Internal ID20818199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:47327952..47328349hg38UCSC Ensembl
chr1:47793624..47794021hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg38398
hg19398
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6540697
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18251159
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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