A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4745619



Internal ID20521629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61340318..61340658hg38UCSC Ensembl
chr11:61107790..61108130hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38341
hg19341
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16281304
Samples
Known GenesDAK
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4745619
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