A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3996048



Internal ID18845163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:12922195..12922467hg38UCSC Ensembl
Outerchr11:12943742..12944014hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38273
hg19273
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1150574
Supporting Variants
SamplesKWB1
Known GenesTEAD1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3996048
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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