A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2998180



Internal ID16944446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:45112550..45126749hg38UCSC Ensembl
Outerchr11:45134101..45148300hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3814200
hg1914200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv951607
Supporting Variants
SamplesBILGI_BIOE
Known GenesPRDM11
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2998180
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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