A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113398



Internal ID21296664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:9523439..9529807hg38UCSC Ensembl
Innerchr17:9426756..9433124hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg386369
hg196369
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14098058
Samplessample59
Known GenesSTX8
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113398
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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