A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867786



Internal ID22642721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:4682760..4682831hg38UCSC Ensembl
chr1:4742820..4742891hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17381779
Samples
Known GenesAJAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867786
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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