A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5973162



Internal ID22748097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1647913..1647913hg38UCSC Ensembl
chr11:1669143..1669143hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38179
hg19179
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17354742
Samples
Known GenesMOB2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5973162
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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