A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv778983



Internal ID16072939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:71113917..71174123hg38UCSC Ensembl
Innerchr11:70824963..70885169hg19UCSC Ensembl
Innerchr11:70502611..70562817hg18UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg3860207
hg1960207
hg1860207
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555400
Supporting Variants
Samples
Known GenesSHANK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv778983
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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