A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1143696



Internal ID19254645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:130159705..130160205hg38UCSC Ensembl
Outerchr11:130029600..130030100hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3994385
SamplesKWS1
Known GenesST14
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1143696
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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