A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5926151



Internal ID22701378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:38078026..38078356hg38UCSC Ensembl
chr11:38099576..38099906hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17352697
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5926151
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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