A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1126299



Internal ID19253921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:68750732..68751532hg38UCSC Ensembl
Outerchr11:68518200..68519000hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg38801
hg19801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv670n106
Supporting Variantsnssv3984535
SamplesKWS1
Known GenesMTL5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1126299
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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