A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5639811



Internal ID21588116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:31361978..31361978hg38UCSC Ensembl
chr10:31650907..31650907hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg38160
hg19160
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17069662
SamplesHG02587
Known GenesZEB1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5639811
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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