A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1113386



Internal ID18922515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:46014684..46015031hg38UCSC Ensembl
Outerchr11:46036235..46036582hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38348
hg19348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3970461, nssv3985553
SamplesKWS2, KWS1
Known GenesPHF21A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1113386
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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