A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5894571



Internal ID22669644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13882318..13883620hg38UCSC Ensembl
chr6:13882549..13883851hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg381303
hg191303
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17410648
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5894571
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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