A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18249880



Internal ID20816921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:118458667..118506730hg38UCSC Ensembl
chr1:119001290..119049353hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg3848064
hg1948064
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6537092
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18249880
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.0001


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