A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6007406



Internal ID21916749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38903996..38908788hg38UCSC Ensembl
chr8:38761514..38766306hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg384793
hg194793
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17566059
Samples
Known GenesPLEKHA2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6007406
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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