A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5661762



Internal ID21610067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:29537703..29537703hg38UCSC Ensembl
chr19:30028610..30028610hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17104253
SamplesNA18939
Known GenesVSTM2B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5661762
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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