A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5565516



Internal ID21513830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15791207..15791284hg38UCSC Ensembl
chr4:15792830..15792907hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17120293
SamplesHG03125
Known GenesCD38
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5565516
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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