A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5613092



Internal ID21561397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:39072186..39072186hg38UCSC Ensembl
chr4:39073806..39073806hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17131357
SamplesNA19238
Known GenesKLHL5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5613092
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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