A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5649953



Internal ID21598258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57125642..57125642hg38UCSC Ensembl
chr19:57637010..57637010hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38341
hg19341
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17106460
SamplesHG00512
Known GenesUSP29
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5649953
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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