A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18273787



Internal ID20840827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156787789..156788805hg38UCSC Ensembl
chr7:156580483..156581499hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg381017
hg191017
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6555671
Supporting Variants
Samples
Known GenesLMBR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18273787
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00012


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