A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553946



Internal ID15994669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:30194611..30260631hg38UCSC Ensembl
Innerchr11:30216158..30282178hg19UCSC Ensembl
Innerchr11:30172734..30238754hg18UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3866021
hg1966021
hg1866021
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv770671
Samples
Known GenesFSHB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553946
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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