A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553405



Internal ID16340814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:7322531..7348644hg38UCSC Ensembl
Innerchr11:7343762..7369875hg19UCSC Ensembl
Innerchr11:7300338..7326451hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3826114
hg1926114
hg1826114
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174293
SamplesHGDP00039
Known GenesSYT9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553405
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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