A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555444



Internal ID15996167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:74489694..74510125hg38UCSC Ensembl
Innerchr11:74200739..74221170hg19UCSC Ensembl
Innerchr11:73878387..73898818hg18UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3820432
hg1920432
hg1820432
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv779219
Samples
Known GenesLIPT2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555444
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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