A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv907521



Internal ID6269448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:1651780..1687796hg19UCSC Ensembl
Outerchr17:1648294..1689657hg19UCSC Ensembl
Innerchr17:1598530..1634546hg18UCSC Ensembl
Outerchr17:1595044..1636407hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1542039
SamplesMS15601
Known GenesSERPINF1, SERPINF2, SMYD4
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv907521
Frequency
Sample Size6533
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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