A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17599931



Internal ID21791978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:21556864..21557247hg38UCSC Ensembl
chr12:21709798..21710181hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg38384
hg19384
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6104159
Supporting Variants
Samples
Known GenesGYS2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17599931
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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