A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6106597



Internal ID22015831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16069538..16069538hg38UCSC Ensembl
chr19:16180348..16180348hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17620660
Samples
Known GenesTPM4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6106597
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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