A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5926708



Internal ID22701935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64416030..64416145hg38UCSC Ensembl
chr11:64183502..64183617hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17358953
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5926708
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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