A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv876886



Internal ID6283897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:63611060..63883671hg19UCSC Ensembl
Outerchr3:63603510..63893477hg19UCSC Ensembl
Innerchr3:63586100..63858711hg18UCSC Ensembl
Outerchr3:63578550..63868517hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1548604
SamplesMS17878
Known GenesATXN7, C3orf49, SNTN, THOC7
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv876886
Frequency
Sample Size6533
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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