A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4739414



Internal ID20515387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:38206765..38206897hg38UCSC Ensembl
chr9:38206762..38206894hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg38133
hg19133
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16259940
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4739414
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