A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5907229



Internal ID22682434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:14403001..14403082hg38UCSC Ensembl
chr5:14403110..14403191hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17418028
Samples
Known GenesTRIO
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5907229
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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