A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18271434



Internal ID20838474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:40956027..40988126hg38UCSC Ensembl
chr6:40923766..40955865hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3832100
hg1932100
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6558522
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18271434
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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