A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv777163



Internal ID16071119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:64627212..64641174hg38UCSC Ensembl
Innerchr11:64394684..64408646hg19UCSC Ensembl
Innerchr11:64151260..64165222hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3813963
hg1913963
hg1813963
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555199
Supporting Variants
Samples
Known GenesNRXN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv777163
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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