A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5902072



Internal ID22677226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:41036860..41040481hg38UCSC Ensembl
chr6:41004599..41008220hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg383622
hg193622
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17436277
Samples
Known GenesUNC5CL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5902072
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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