A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552770



Internal ID15993493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:356090..444628hg38UCSC Ensembl
Innerchr11:356090..444628hg19UCSC Ensembl
Innerchr11:346090..434628hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3888539
hg1988539
hg1888539
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv763053
Samples
Known GenesANO9, B4GALNT4, PKP3, SIGIRR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552770
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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