A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5612738



Internal ID21561043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:68329643..68329643hg38UCSC Ensembl
chr4:69195361..69195361hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17125944
SamplesHG03065
Known GenesYTHDC1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5612738
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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