A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5617878



Internal ID21566183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9535562..9535562hg38UCSC Ensembl
chr3:9577246..9577246hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17133664
SamplesHG00513
Known GenesLHFPL4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5617878
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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