A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5614826



Internal ID21563131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:159355943..159355943hg38UCSC Ensembl
chr3:159073732..159073732hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17138900
SamplesHG03125
Known GenesIQCJ-SCHIP1, SCHIP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5614826
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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