A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18247908



Internal ID20814948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:212052610..212055204hg38UCSC Ensembl
chr1:212225952..212228546hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg382595
hg192595
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6553852
Supporting Variants
Samples
Known GenesDTL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18247908
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00136


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