A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5920195



Internal ID22695418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:31838448..31838975hg38UCSC Ensembl
chr11:31859995..31860522hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38528
hg19528
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17352346
Samples
Known GenesDKFZp686K1684
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5920195
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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