A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv877390



Internal ID6284401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:121990257..122020194hg19UCSC Ensembl
Outerchr3:121988355..122030601hg19UCSC Ensembl
Innerchr3:123472947..123502884hg18UCSC Ensembl
Outerchr3:123471045..123513291hg18UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1548654
SamplesMS17878
Known GenesCASR
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv877390
Frequency
Sample Size6533
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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