A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18250253



Internal ID20817293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:193924814..193925599hg38UCSC Ensembl
chr1:193893944..193894729hg19UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg38786
hg19786
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6550076
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18250253
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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