A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18276646



Internal ID20843686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:77814539..77815075hg38UCSC Ensembl
chr7:77443856..77444392hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38537
hg19537
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6569480
Supporting Variants
Samples
Known GenesPHTF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18276646
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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