A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951609



Internal ID16953796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:45992450..46014749hg38UCSC Ensembl
Outerchr11:46014001..46036300hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3822300
hg1922300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999509
SamplesBILGI_BIOE
Known GenesPHF21A
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951609
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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