A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5587586



Internal ID21536144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:17828147..17832657hg38UCSC Ensembl
chr10:17870146..17874656hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg384511
hg194511
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17069479
SamplesHG03065
Known GenesMRC1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5587586
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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