A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18252369



Internal ID20819409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:29552252..30655895hg38UCSC Ensembl
chr1:30028083..31128742hg19UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg381103644
hg191100660
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6548662
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18252369
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.49972


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