A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5906238



Internal ID22681435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15841532..15847618hg38UCSC Ensembl
chr4:15843155..15849241hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg386087
hg196087
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17419602
Samples
Known GenesCD38
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5906238
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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