A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5661855



Internal ID21610160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2939008..2939008hg38UCSC Ensembl
chr19:2939006..2939006hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38245
hg19245
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17104369
SamplesHG00513
Known GenesZNF77
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5661855
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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