A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17066199



Internal ID21488419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:64239074..64239074hg38UCSC Ensembl
chr1:64704757..64704757hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38357
hg19357
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5620793
Supporting Variants
SamplesNA18939
Known GenesUBE2U
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17066199
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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