A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18248300



Internal ID20815340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:201094950..201096885hg38UCSC Ensembl
chr1:201064078..201066013hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg381936
hg191936
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6537775
Supporting Variants
Samples
Known GenesCACNA1S
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18248300
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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