A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951305



Internal ID17300179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:7701254..7716553hg38UCSC Ensembl
Outerchr11:7722801..7738100hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3815300
hg1915300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998147
SamplesBILGI_BIOE
Known GenesOVCH2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951305
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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