A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1120653



Internal ID18936032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:45111273..45111436hg38UCSC Ensembl
Outerchr11:45132824..45132987hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3963084
SamplesKWS2
Known GenesPRDM11
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1120653
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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