A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5585302



Internal ID21533848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:45377950..45378029hg38UCSC Ensembl
chr13:45952085..45952164hg19UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17087664
SamplesHG00731
Known GenesTPT1-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5585302
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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