A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv779868



Internal ID16073824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:85008976..85033882hg38UCSC Ensembl
Innerchr11:84720020..84744926hg19UCSC Ensembl
Innerchr11:84397668..84422574hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3824907
hg1924907
hg1824907
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555629
Supporting Variants
Samples
Known GenesDLG2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv779868
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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