A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18248756



Internal ID20815796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:17488193..17488670hg38UCSC Ensembl
chr1:17814689..17815166hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38478
hg19478
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6546533
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18248756
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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