A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5915642



Internal ID22690860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:7211922..7220253hg38UCSC Ensembl
chr11:7233153..7241484hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg388332
hg198332
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17353893
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5915642
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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