A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv905153



Internal ID6267080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:2510603..2585875hg19UCSC Ensembl
Outerchr16:2506306..2595303hg19UCSC Ensembl
Innerchr16:2450604..2525876hg18UCSC Ensembl
Outerchr16:2446307..2535304hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1510919
SamplesSP54988
Known GenesAMDHD2, ATP6V0C, C16orf59, CCNF, CEMP1, MIR3178, NTN3, PDPK1, TBC1D24
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv905153
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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