A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18275871



Internal ID20842911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99925189..99936027hg38UCSC Ensembl
chr7:99522812..99533650hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3810839
hg1910839
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6568326
Supporting Variants
Samples
Known GenesGJC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18275871
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00036


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