A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5927831



Internal ID22703063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41573815..41577884hg38UCSC Ensembl
chr15:41866013..41870082hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg384070
hg194070
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17376597
Samples
Known GenesTYRO3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5927831
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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