A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv877465



Internal ID6284476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:128516142..128670446hg19UCSC Ensembl
Outerchr3:128499195..128691941hg19UCSC Ensembl
Innerchr3:129998832..130153136hg18UCSC Ensembl
Outerchr3:129981885..130174631hg18UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1548668
SamplesMS17878
Known GenesACAD9, KIAA1257, LOC653712, RAB7A
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv877465
Frequency
Sample Size6533
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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