A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv773970



Internal ID16067926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:49986721..50683379hg38UCSC Ensembl
Innerchr11:50008258..50642550hg19UCSC Ensembl
Innerchr11:49964834..50599126hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38696659
hg19634293
hg18634293
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv554395
Supporting Variants
Samples
Known GenesLOC441601, LOC646813
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv773970
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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