A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17464739



Internal ID22522627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:44453630..44454629hg38UCSC Ensembl
chr13:45027766..45028765hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5864334
Supporting Variants
Samples
Known GenesTSC22D1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17464739
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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