A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18253141



Internal ID20820181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:76062516..76063126hg38UCSC Ensembl
chr1:76528201..76528811hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38611
hg19611
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6545473
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18253141
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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