A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5606084



Internal ID21554389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150506578..150506578hg38UCSC Ensembl
chr1:150479054..150479054hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17061135, nssv17061136
SamplesHG03065, HG00731
Known GenesTARS2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5606084
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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