A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5928363



Internal ID22703601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40867515..40871092hg38UCSC Ensembl
chr15:41159713..41163290hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg383578
hg193578
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17381544
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5928363
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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