A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5917418



Internal ID22692637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:83126526..83135085hg38UCSC Ensembl
chr11:82837568..82846127hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg388560
hg198560
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17358078
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5917418
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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