A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5585389



Internal ID21533935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42350281..42350806hg38UCSC Ensembl
chr15:42642479..42643004hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38526
hg19526
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17079744
SamplesHG02011
Known GenesGANC
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5585389
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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