A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5586022



Internal ID21534571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:122633342..122633406hg38UCSC Ensembl
chr10:124392858..124392922hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17068602
SamplesHG00732
Known GenesDMBT1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5586022
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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