A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5615461



Internal ID21563766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:10812..10812hg38UCSC Ensembl
chr4:10812..10812hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17120130
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5615461
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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