A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18275793



Internal ID20842833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98026802..98408454hg38UCSC Ensembl
chr7:97656114..98037766hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38381653
hg19381653
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6567614
Supporting Variants
Samples
Known GenesBAIAP2L1, BHLHA15, BRI3, LMTK2, TECPR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18275793
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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