A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5625512



Internal ID21573817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:168034123..168034123hg38UCSC Ensembl
chr5:167461128..167461128hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17134363
SamplesNA19238
Known GenesTENM2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5625512
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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