A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5906225



Internal ID22681422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:95409283..95409459hg38UCSC Ensembl
chr5:94744987..94745163hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38177
hg19177
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17424539
Samples
Known GenesFAM81B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5906225
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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