A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5616277



Internal ID21564582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:31351464..31351464hg38UCSC Ensembl
chr4:31353086..31353086hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17120736
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5616277
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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