A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5579071



Internal ID21527547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:36283616..36283667hg38UCSC Ensembl
chr1:36749217..36749268hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17064817
SamplesHG00731
Known GenesTHRAP3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5579071
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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