A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5610103



Internal ID21558408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:15611566..15611566hg38UCSC Ensembl
chr2:15751690..15751690hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17110512
SamplesHG00513
Known GenesDDX1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5610103
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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