A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5585405



Internal ID21533952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14933455..15015970hg38UCSC Ensembl
chr10:14975454..15057969hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3882516
hg1982516
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17069214
SamplesHG03683
Known GenesDCLRE1C, MEIG1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5585405
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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