A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5935281



Internal ID22710620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:83441394..83441493hg38UCSC Ensembl
chr15:84110146..84110245hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17376108
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5935281
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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