A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18272205



Internal ID20839245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:104205223..104205772hg38UCSC Ensembl
chr7:103845671..103846220hg19UCSC Ensembl
Cytoband7q22.2
Allele length
AssemblyAllele length
hg38550
hg19550
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6562363
Supporting Variants
Samples
Known GenesORC5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18272205
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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