A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18249958



Internal ID20816998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:204792835..204794092hg38UCSC Ensembl
chr1:204761963..204763220hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg381258
hg191258
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6551359
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18249958
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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