A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5900009



Internal ID22675146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:146412871..146413845hg38UCSC Ensembl
chr5:145792434..145793408hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38975
hg19975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17419806
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5900009
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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