A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18249689



Internal ID20816729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:52065268..52066050hg38UCSC Ensembl
chr1:52530940..52531722hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg38783
hg19783
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6554272
Supporting Variants
Samples
Known GenesBTF3L4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18249689
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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