A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv906907



Internal ID6268834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:74735148..74778006hg19UCSC Ensembl
Outerchr16:74702254..74785902hg19UCSC Ensembl
Innerchr16:73292649..73335507hg18UCSC Ensembl
Outerchr16:73259755..73343403hg18UCSC Ensembl
Cytoband16q22.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1530846
SamplesMS10311
Known GenesFA2H, MLKL
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv906907
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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