A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17598771



Internal ID21790816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:51682395..51685717hg38UCSC Ensembl
chr13:52256531..52259853hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg383323
hg193323
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6106926
Supporting Variants
Samples
Known GenesWDFY2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17598771
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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