A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv904138



Internal ID6266065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:43276345..43403955hg19UCSC Ensembl
Outerchr15:43268970..43414673hg19UCSC Ensembl
Innerchr15:41063637..41191247hg18UCSC Ensembl
Outerchr15:41056262..41201965hg18UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain+Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnssv1596713, nssv1569351
SamplesIS31563, IS40618
Known GenesUBR1
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv904138
Frequency
Sample Size6533
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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