A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5888996



Internal ID22664007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:38777230..38777359hg38UCSC Ensembl
chr4:38778851..38778980hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17409686
Samples
Known GenesTLR10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5888996
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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