A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5968720



Internal ID22743655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:55988484..55988484hg38UCSC Ensembl
chr15:56280682..56280682hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38199
hg19199
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17383676
Samples
Known GenesNEDD4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5968720
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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