A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3963534



Internal ID18861449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:45111212..45111405hg38UCSC Ensembl
Outerchr11:45132763..45132956hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38194
hg19194
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1130306
Supporting Variants
SamplesKWS1
Known GenesPRDM11
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3963534
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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