A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv904334



Internal ID6266261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:71742406..72154000hg19UCSC Ensembl
Outerchr15:71737376..72177659hg19UCSC Ensembl
Innerchr15:69529460..69941054hg18UCSC Ensembl
Outerchr15:69524430..69964713hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1540337
SamplesMS14805
Known GenesMYO9A, NR2E3, THSD4
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv904334
Frequency
Sample Size6533
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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