A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5945320



Internal ID22720795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41569019..41570022hg38UCSC Ensembl
chr15:41861217..41862220hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg381004
hg191004
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17371585
Samples
Known GenesTYRO3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5945320
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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