A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5575836



Internal ID21524268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:151081299..151081348hg38UCSC Ensembl
chr3:150799086..150799135hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17129738
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5575836
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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