A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117328



Internal ID21300594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:84026174..84096073hg38UCSC Ensembl
Innerchr15:84694926..84764825hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3869900
hg1969900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14098199
Samplessample423
Known GenesADAMTSL3, EFTUD1P1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117328
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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