A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5906478



Internal ID22681679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:24393002..24396301hg38UCSC Ensembl
chr5:24393111..24396410hg19UCSC Ensembl
Cytoband5p14.2
Allele length
AssemblyAllele length
hg383300
hg193300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17419095
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5906478
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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