A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110803



Internal ID21294069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:37904073..37994204hg38UCSC Ensembl
Innerchr10:38193001..38283132hg19UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg3890132
hg1990132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14088487
Samplessample169
Known GenesZNF25
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110803
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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