A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5893179



Internal ID22668237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:38687164..38687389hg38UCSC Ensembl
chr6:38654940..38655165hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38226
hg19226
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17437840
Samples
Known GenesGLO1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5893179
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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