A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5897293



Internal ID22672394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:40903913..40909335hg38UCSC Ensembl
chr4:40905930..40911352hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg385423
hg195423
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17412585
Samples
Known GenesAPBB2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5897293
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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