A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5606441



Internal ID21554746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156586449..156586449hg38UCSC Ensembl
chr1:156556241..156556241hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg382546
hg192546
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17061188
SamplesNA19239
Known GenesTTC24
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5606441
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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