A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1111409



Internal ID19283999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:68415630..68415937hg38UCSC Ensembl
Outerchr11:68183098..68183405hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv668n106
Supporting Variantsnssv3963533
SamplesKWS1
Known GenesLRP5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1111409
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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