A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5894641



Internal ID22669715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:105929622..105929729hg38UCSC Ensembl
chr4:106850779..106850886hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17412824
Samples
Known GenesNPNT
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5894641
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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