A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5567162



Internal ID21515494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:154632732..154632783hg38UCSC Ensembl
chr4:155553884..155553935hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17126244
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5567162
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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