A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5602107



Internal ID21550761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68269388..68269705hg38UCSC Ensembl
chr15:68561726..68562043hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17085220
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5602107
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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