A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18250447



Internal ID20817487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:60659128..60659854hg38UCSC Ensembl
chr1:61124800..61125526hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg38727
hg19727
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6546091
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18250447
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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