A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5577404



Internal ID21525856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:167102932..167102994hg38UCSC Ensembl
chr1:167072169..167072231hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17061737
SamplesHG00732
Known GenesDUSP27
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5577404
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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