A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5893974



Internal ID22669042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:167379582..167380426hg38UCSC Ensembl
chr5:166806587..166807431hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38845
hg19845
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17419019
Samples
Known GenesTENM2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5893974
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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