A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1149894



Internal ID19200756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:126448804..126451605hg38UCSC Ensembl
Outerchr11:126318699..126321500hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg382802
hg192802
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3998683
SamplesKWB1
Known GenesKIRREL3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1149894
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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