A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867811



Internal ID22642746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:4411686..4412334hg38UCSC Ensembl
chr1:4471746..4472394hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg38649
hg19649
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17385288
Samples
Known GenesLOC284661
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867811
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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