A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18252669



Internal ID20819709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:92130901..92131549hg38UCSC Ensembl
chr1:92596458..92597106hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg38649
hg19649
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6538048
Supporting Variants
Samples
Known GenesBTBD8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18252669
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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