A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18247846



Internal ID20814886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:209754499..209754960hg38UCSC Ensembl
chr1:209927844..209928305hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg38462
hg19462
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6544341
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18247846
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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