A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6102340



Internal ID22011574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11526876..11526876hg38UCSC Ensembl
chr19:11637691..11637691hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17628177
Samples
Known GenesECSIT
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6102340
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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