A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567614



Internal ID20940685
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 StatusM
Merged Variants
Supporting Variantsnssv18275793
Samples
Known GenesBAIAP2L1, BHLHA15, BRI3, LMTK2, TECPR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567614
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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