A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17065409



Internal ID21509291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:5160083..5160083hg38UCSC Ensembl
chr1:5220143..5220143hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg38533
hg19533
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5605304
Supporting Variants
SamplesNA20847
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17065409
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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