A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6105669



Internal ID22014902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:51345743..51345743hg38UCSC Ensembl
chr19:51848997..51848997hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17622571
Samples
Known GenesETFB
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6105669
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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