A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv904304



Internal ID6266231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:63363631..63445144hg19UCSC Ensembl
Outerchr15:63360847..63474391hg19UCSC Ensembl
Innerchr15:61150684..61232197hg18UCSC Ensembl
Outerchr15:61147900..61261444hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1560056
SamplesMS24274
Known GenesLACTB, RPS27L, TPM1
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv904304
Frequency
Sample Size6533
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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