A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5606011



Internal ID21554316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161750900..161750900hg38UCSC Ensembl
chr1:161720690..161720690hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38295
hg19295
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17061048
SamplesHG03732
Known GenesDUSP12
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5606011
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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