A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv889198



Internal ID6296209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:128491284..128497990hg19UCSC Ensembl
Outerchr7:128490999..128499079hg19UCSC Ensembl
Innerchr7:128278520..128285226hg18UCSC Ensembl
Outerchr7:128278235..128286315hg18UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1500455
SamplesSP50159
Known GenesFLNC
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv889198
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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