A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5887558



Internal ID22662550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:213604306..213617435hg38UCSC Ensembl
chr2:214469030..214482159hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg3813130
hg1913130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17409071
Samples
Known GenesSPAG16
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5887558
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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