A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18271591



Internal ID20838631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:102964031..102964671hg38UCSC Ensembl
chr7:102604478..102605118hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38641
hg19641
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6563390
Supporting Variants
Samples
Known GenesFBXL13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18271591
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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