A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18253981



Internal ID20821021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:96141935..96142968hg38UCSC Ensembl
chr1:96607491..96608524hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg381034
hg191034
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6546558
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18253981
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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