A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv949868



Internal ID17298742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:149644865..149652264hg38UCSC Ensembl
Outerchr6:149966001..149973400hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg387400
hg197400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997534
SamplesBILGI_BIOE
Known GenesKATNA1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv949868
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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