A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5907011



Internal ID22682215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:165070659..165077229hg38UCSC Ensembl
chr5:164497665..164504235hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg386571
hg196571
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17424051
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5907011
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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