A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5649161



Internal ID21597466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12093859..12093859hg38UCSC Ensembl
chr19:12204674..12204674hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381478
hg191478
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17103132
SamplesNA19239
Known GenesZNF788
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5649161
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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