A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5584115



Internal ID21532650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:159711196..159711394hg38UCSC Ensembl
chr3:159428985..159429183hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg38199
hg19199
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17122042
SamplesHG00513
Known GenesIQCJ-SCHIP1, SCHIP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5584115
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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