A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5919167



Internal ID22694389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:43981049..43984524hg38UCSC Ensembl
chr11:44002599..44006074hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg383476
hg193476
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17360056
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5919167
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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