A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110691



Internal ID21293957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:25873091..25879064hg38UCSC Ensembl
Innerchr10:26162020..26167993hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg385974
hg195974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14090099
Samplessample115
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110691
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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