A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6038680



Internal ID21948023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:46948466..46949168hg38UCSC Ensembl
chr11:46970017..46970719hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38703
hg19703
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17594470
Samples
Known GenesC11orf49
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6038680
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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