A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv904478



Internal ID6266405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:89414295..89445784hg19UCSC Ensembl
Outerchr15:89410314..89448201hg19UCSC Ensembl
Innerchr15:87215299..87246788hg18UCSC Ensembl
Outerchr15:87211318..87249205hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1530816
SamplesMS10311
Known GenesACAN, HAPLN3, MFGE8
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv904478
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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