A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5656608



Internal ID21604913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:1487230..1487230hg38UCSC Ensembl
chr16:1537231..1537231hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg381152
hg191152
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17098700
SamplesHG01596
Known GenesPTX4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5656608
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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