A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5610121



Internal ID21558426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:168725215..168725215hg38UCSC Ensembl
chr1:168694453..168694453hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17061278
SamplesHG00732
Known GenesDPT
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5610121
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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