A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5908754



Internal ID22683964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:34496552..34499113hg38UCSC Ensembl
chr11:34518099..34520660hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg382562
hg192562
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17364342
Samples
Known GenesELF5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5908754
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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