A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3971651



Internal ID18879521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:102374819..102374877hg38UCSC Ensembl
Outerchr11:102245550..102245608hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1134170
Supporting Variants
SamplesKWS2
Known GenesBIRC2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3971651
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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