A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv904100



Internal ID6266027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:40966765..40990353hg19UCSC Ensembl
Outerchr15:40959624..40994706hg19UCSC Ensembl
Innerchr15:38754057..38777645hg18UCSC Ensembl
Outerchr15:38746916..38781998hg18UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1510092
SamplesSP54956
Known GenesLOC100505648, RAD51
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv904100
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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