A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv949883



Internal ID16952070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:161056969..161062868hg38UCSC Ensembl
Outerchr6:161478001..161483900hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg385900
hg195900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997549
SamplesBILGI_BIOE
Known GenesMAP3K4
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv949883
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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