A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5923882



Internal ID22699109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:34117308..34140658hg38UCSC Ensembl
chr11:34138855..34162205hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3823351
hg1923351
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17350400
Samples
Known GenesNAT10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5923882
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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