A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17607396



Internal ID21799443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:79904982..79905289hg38UCSC Ensembl
chr15:80197324..80197631hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6102337
Supporting Variants
Samples
Known GenesST20, ST20-MTHFS
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17607396
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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