A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6046689



Internal ID21955922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:47747964..47748108hg38UCSC Ensembl
chr19:48251221..48251365hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg38145
hg19145
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17620574
Samples
Known GenesGLTSCR2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6046689
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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