A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv774849



Internal ID16068805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:54944514..55118209hg38UCSC Ensembl
Innerchr11:54711990..54885685hg19UCSC Ensembl
Innerchr11:54468566..54642261hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38173696
hg19173696
hg18173696
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv554658
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv774849
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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