A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3005102



Internal ID17298054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:46386982..46387128hg38UCSC Ensembl
Outerchr11:46408532..46408678hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38147
hg19147
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv957373
Supporting Variants
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3005102
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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