A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv889087



Internal ID6296098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:117229167..117241394hg19UCSC Ensembl
Outerchr7:117226766..117246315hg19UCSC Ensembl
Innerchr7:117016403..117028630hg18UCSC Ensembl
Outerchr7:117014002..117033551hg18UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnssv1582965, nssv1579634, nssv1567394, nssv1535573, nssv1582356, nssv1581844, nssv1565716
SamplesIS30508, IS35911, IS36219, IS35742, IS35145, MS12266, IS31074
Known GenesCFTR
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv889087
Frequency
Sample Size6533
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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