A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5924255



Internal ID22699482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9361050..9363833hg38UCSC Ensembl
chr11:9382597..9385380hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg382784
hg192784
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17351568
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5924255
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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