A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5900029



Internal ID22675167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:167912478..167916645hg38UCSC Ensembl
chr5:167339483..167343650hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg384168
hg194168
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17427657
Samples
Known GenesTENM2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5900029
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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