A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5576899



Internal ID21525344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:171780097..171780190hg38UCSC Ensembl
chr3:171497887..171497980hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17127765
SamplesNA19239
Known GenesPLD1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5576899
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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