A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17615533



Internal ID21807580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:73706334..73706334hg38UCSC Ensembl
chr13:74280471..74280471hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6098876
Supporting Variants
Samples
Known GenesKLF12
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17615533
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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