A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5879499



Internal ID22654468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:211423768..211438213hg38UCSC Ensembl
chr1:211597110..211611555hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg3814446
hg1914446
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17355246
Samples
Known GenesLINC00467
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5879499
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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