A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18274406



Internal ID20841446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139134455..139135104hg38UCSC Ensembl
chr7:138819201..138819850hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38650
hg19650
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6565501
Supporting Variants
Samples
Known GenesTTC26
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18274406
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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