A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5572030



Internal ID21520414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:150366628..150366953hg38UCSC Ensembl
chr5:149746191..149746516hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17139073
SamplesHG00732
Known GenesTCOF1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5572030
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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