A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18250339



Internal ID20817379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:229793207..229794043hg38UCSC Ensembl
chr1:229928954..229929790hg19UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg38837
hg19837
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6550599
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18250339
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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