A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv905152



Internal ID6267079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:2512523..2985358hg19UCSC Ensembl
Outerchr16:2484783..2992114hg19UCSC Ensembl
Innerchr16:2452524..2925359hg18UCSC Ensembl
Outerchr16:2424784..2932115hg18UCSC 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 Variantsnssv1546888
SamplesMS17208
Known GenesAMDHD2, ATP6V0C, C16orf59, CCNF, CEMP1, FLJ42627, FLYWCH1, FLYWCH2, KCTD5, LOC100128788, LOC100507321, LOC652276, MIR3178, NTN3, PDPK1, PRSS21, PRSS22, PRSS27, PRSS30P, PRSS33, PRSS41, SRRM2, TBC1D24, TCEB2, ZG16B
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv905152
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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