A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv949886



Internal ID16952073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:163416369..163458368hg38UCSC Ensembl
Outerchr6:163837401..163879400hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3842000
hg1942000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997552
SamplesBILGI_BIOE
Known GenesQKI
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv949886
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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