A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4766573



Internal ID20542433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:19098513..19098513hg38UCSC Ensembl
chr7:19138136..19138136hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16290370
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4766573
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer