A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5874882



Internal ID22649836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15063837..15063891hg38UCSC Ensembl
chr1:15390333..15390387hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17365720
Samples
Known GenesKAZN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5874882
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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