A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5600146



Internal ID21548784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:38018936..38019482hg38UCSC Ensembl
chr10:38307864..38308410hg19UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg38547
hg19547
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17070185
SamplesHG03371
Known GenesZNF33A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5600146
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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