A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027977



Internal ID21937320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:68876137..68876523hg38UCSC Ensembl
chr11:68643605..68643991hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg38387
hg19387
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17583837
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027977
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