A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18275942



Internal ID20842982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:41995606..41995706hg38UCSC Ensembl
chr7:42035205..42035305hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6564616
Supporting Variants
Samples
Known GenesGLI3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18275942
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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