A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv949881



Internal ID17298755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:160612969..160646468hg38UCSC Ensembl
Outerchr6:161034001..161067500hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3833500
hg1933500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997547
SamplesBILGI_BIOE
Known GenesLPA
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv949881
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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