A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4746277



Internal ID20522289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:138029292..138029352hg38UCSC Ensembl
chr6:138350429..138350489hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16266495
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4746277
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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