A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17703041



Internal ID126707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:49468895..49474634hg38UCSC Ensembl
chr15:49761092..49766831hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg385740
hg195740
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5562138
Supporting Variants
Samples
Known GenesFAM227B, FGF7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17703041
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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