A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18276926



Internal ID20843966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:92663637..92664829hg38UCSC Ensembl
chr7:92292951..92294143hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg381193
hg191193
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6573644
Supporting Variants
Samples
Known GenesCDK6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18276926
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00032


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