A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5662272



Internal ID21610577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3937900..3937900hg38UCSC Ensembl
chr19:3937898..3937898hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38184
hg19184
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17104709, nssv17104708
SamplesNA19239, HG03683
Known GenesNMRK2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5662272
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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