A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv820731



Internal ID6111440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:40489925..40490615hg19UCSC Ensembl
Innerchr17:37743451..37744141hg18UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Deletion
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1419936
SamplesNA10851
Known GenesSTAT3
Method
AnalysisIdentical to variant call (no regions submitted)
PlatformIllumina IIx
Comments
ReferenceJu_et_al_2010
Pubmed ID20802225
Accession Number(s)nsv820731
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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