A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5649903



Internal ID21598208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10519358..10519358hg38UCSC Ensembl
chr16:10613215..10613215hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17098307
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5649903
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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