A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv767051



Internal ID16061007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:8937356..8938710hg38UCSC Ensembl
Innerchr11:8958903..8960257hg19UCSC Ensembl
Innerchr11:8915479..8916833hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381355
hg191355
hg181355
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553448
Supporting Variants
Samples
Known GenesASCL3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv767051
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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