A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18248068



Internal ID20815108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:169115172..169115344hg38UCSC Ensembl
chr1:169084410..169084582hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg38173
hg19173
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6553591
Supporting Variants
Samples
Known GenesATP1B1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18248068
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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