A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18275855



Internal ID20842895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99513440..99513902hg38UCSC Ensembl
chr7:99111063..99111525hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38463
hg19463
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6558884
Supporting Variants
Samples
Known GenesZKSCAN5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18275855
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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