A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4437151



Internal ID22103329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:116678718..116679434hg38UCSC Ensembl
chr8:117690957..117691673hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg38717
hg19717
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15760649
Samples
Known GenesEIF3H
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4437151
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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