A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17064736



Internal ID21433931
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 StatusS
Merged Variantsnsv5573708
Supporting Variants
SamplesHG00731
Known GenesPTP4A2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17064736
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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