A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv896767



Internal ID6303778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:1987045..2040997hg19UCSC Ensembl
Outerchr11:1985127..2043867hg19UCSC Ensembl
Innerchr11:1943621..1997573hg18UCSC Ensembl
Outerchr11:1941703..2000443hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1572657
SamplesIS33162
Known GenesH19, MIR675, MRPL23-AS1
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv896767
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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