A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17605036



Internal ID21797083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:29558228..29558228hg38UCSC Ensembl
chr13:30132365..30132365hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6097679
Supporting Variants
Samples
Known GenesSLC7A1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17605036
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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