A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5929423



Internal ID22704676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:91720037..91733313hg38UCSC Ensembl
chr15:92263267..92276543hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3813277
hg1913277
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17387828
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5929423
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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