A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5583414



Internal ID21531939
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 Variantsnssv17130641
SamplesHG03125
Known GenesCD38
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5583414
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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