A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4738760



Internal ID20514731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:47262283..47262371hg38UCSC Ensembl
chr19:47765540..47765628hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16285354
Samples
Known GenesCCDC9
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4738760
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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