A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5625771



Internal ID21574076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:34298468..34298468hg38UCSC Ensembl
chr6:34266245..34266245hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17155467
SamplesNA19238
Known GenesNUDT3, RPS10-NUDT3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5625771
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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