A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18273806



Internal ID20840846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:157375919..158261000hg38UCSC Ensembl
chr7:157168613..158053692hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38885082
hg19885080
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6562942
Supporting Variants
Samples
Known GenesDNAJB6, LOC100506585, MIR153-2, PTPRN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18273806
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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