A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5927883



Internal ID22703116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:83614555..83708505hg38UCSC Ensembl
chr15:84283307..84377257hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3893951
hg1993951
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17378537
Samples
Known GenesADAMTSL3, SH3GL3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5927883
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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