A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv907223



Internal ID6269150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88364483..88552370hg19UCSC Ensembl
Outerchr16:88355252..88554907hg19UCSC Ensembl
Innerchr16:86921984..87079871hg18UCSC Ensembl
Outerchr16:86912753..87082408hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1537144
SamplesMS13095
Known GenesZFPM1, ZNF469
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv907223
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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