A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5875486



Internal ID22650443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:14331214..14331989hg38UCSC Ensembl
chr1:14657709..14658484hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg38776
hg19776
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17368197
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5875486
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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