A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4433154



Internal ID21395156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:62686046..62686419hg38UCSC Ensembl
chr1:63151717..63152090hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38374
hg19374
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15752404
SamplesMDQ045
Known GenesDOCK7
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4433154
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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