A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5580673



Internal ID21529166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:40735763..40740479hg38UCSC Ensembl
chr5:40735865..40740581hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg384717
hg194717
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17125204
SamplesNA19650
Known GenesTTC33
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5580673
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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