A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6106897



Internal ID22016130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44000057..44000057hg38UCSC Ensembl
chr19:44504209..44504209hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17624188
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6106897
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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