A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5978373



Internal ID22753308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:72278302..72278302hg38UCSC Ensembl
chr11:71989346..71989346hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38693
hg19693
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17350264
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5978373
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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