A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv904267



Internal ID6266194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:58706846..58763678hg19UCSC Ensembl
Outerchr15:58699010..58769583hg19UCSC Ensembl
Innerchr15:56494138..56550970hg18UCSC Ensembl
Outerchr15:56486302..56556875hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1539462
SamplesMS14334
Known GenesLIPC
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv904267
Frequency
Sample Size6533
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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