A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv886540



Internal ID6293551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:111538387..111580561hg19UCSC Ensembl
Outerchr6:111537481..111590094hg19UCSC Ensembl
Innerchr6:111645080..111687254hg18UCSC Ensembl
Outerchr6:111644174..111696787hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1570240
SamplesIS31837
Known GenesKIAA1919, SLC16A10
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv886540
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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