A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5891187



Internal ID22666222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:183715941..183717225hg38UCSC Ensembl
chr3:183433729..183435013hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg381285
hg191285
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17410545
Samples
Known GenesYEATS2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5891187
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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