A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv906906



Internal ID6268833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:74670458..74801310hg19UCSC Ensembl
Outerchr16:74664743..74805668hg19UCSC Ensembl
Innerchr16:73227959..73358811hg18UCSC Ensembl
Outerchr16:73222244..73363169hg18UCSC Ensembl
Cytoband16q22.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1518398
SamplesSP57545
Known GenesFA2H, MLKL, RFWD3
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv906906
Frequency
Sample Size6533
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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