A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18249332



Internal ID20816372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:223692687..223693283hg38UCSC Ensembl
chr1:223880389..223880985hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38597
hg19597
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6549220
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18249332
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00012


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