A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5917992



Internal ID22693213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95150475..95151027hg38UCSC Ensembl
chr11:94883639..94884191hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38553
hg19553
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17352141
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5917992
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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