A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5610030



Internal ID21558335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:202992011..202992011hg38UCSC Ensembl
chr1:202961139..202961139hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17062580
SamplesNA20847
Known GenesLOC401980
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5610030
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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