A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4749548



Internal ID20525580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:63339349..63340809hg38UCSC Ensembl
chr10:65099109..65100569hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg381461
hg191461
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16268754
Samples
Known GenesJMJD1C
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4749548
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