A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115740



Internal ID21299006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:40816989..40820985hg38UCSC Ensembl
Innerchr17:38973241..38977237hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg383997
hg193997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv491n145
Supporting Variantsnssv14097790
Samplessample289
Known GenesKRT10, TMEM99
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115740
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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