A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5915156



Internal ID22690374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9028475..9028528hg38UCSC Ensembl
chr11:9050022..9050075hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17350444
Samples
Known GenesSCUBE2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5915156
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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