A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1111892



Internal ID18940468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:132213718..132214032hg38UCSC Ensembl
Outerchr11:132083612..132083926hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv739n106
Supporting Variantsnssv3964987, nssv3989006
SamplesKWS2, KWS1
Known GenesNTM
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1111892
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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