A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv949867



Internal ID17298741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:149318965..149356764hg38UCSC Ensembl
Outerchr6:149640101..149677900hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3837800
hg1937800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997533
SamplesBILGI_BIOE
Known GenesTAB2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv949867
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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