A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5573708



Internal ID21522116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:31908111..31908196hg38UCSC Ensembl
chr1:32373712..32373797hg19UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17064736
SamplesHG00731
Known GenesPTP4A2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5573708
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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