A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18249613



Internal ID20816653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:190487842..190488004hg38UCSC Ensembl
chr1:190456972..190457134hg19UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg38163
hg19163
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6554460
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18249613
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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