A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5917857



Internal ID22693078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:86573497..86573703hg38UCSC Ensembl
chr11:86284539..86284745hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg38207
hg19207
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17356956
Samples
Known GenesME3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5917857
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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