A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5915044



Internal ID22690262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:117396806..117397093hg38UCSC Ensembl
chr10:119156317..119156604hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38288
hg19288
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17366073
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5915044
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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