A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18248536



Internal ID20815576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:212877421..212878413hg38UCSC Ensembl
chr1:213050763..213051755hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg38993
hg19993
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6549852
Supporting Variants
Samples
Known GenesFLVCR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18248536
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00015


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