A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5979638



Internal ID22754573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:82946817..82946817hg38UCSC Ensembl
chr11:82657859..82657859hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17359507
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5979638
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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