A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5900803



Internal ID22675949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:81981415..81987555hg38UCSC Ensembl
chr5:81277234..81283374hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg386141
hg196141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17413202
Samples
Known GenesATG10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5900803
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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