A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4731819



Internal ID20507740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:38144170..38144227hg38UCSC Ensembl
chr6:38111946..38112003hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16294780
Samples
Known GenesZFAND3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4731819
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