A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6109314



Internal ID22018547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:7870499..7870499hg38UCSC Ensembl
chr19:7935385..7935385hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38379
hg19379
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17633015
Samples
Known GenesFLJ22184
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6109314
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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