A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6110676



Internal ID22019909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:5673937..5673937hg38UCSC Ensembl
chr19:5673948..5673948hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17623435
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6110676
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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