A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17002929



Internal ID69569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99925192..99936027hg38UCSC Ensembl
chr7:99522815..99533650hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3810836
hg1910836
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5557232
Supporting Variants
Samples
Known GenesGJC3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17002929
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.002342


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