A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2570n71



Internal ID6320190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2446021..2812939hg19UCSC Ensembl
chr16:2386022..2752940hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv905150, nsv905151, nsv905147
SamplesIS33684, IS37646, MS16153, MS18276
Known GenesABCA17P, AMDHD2, ATP6V0C, C16orf59, CCNF, CEMP1, FLJ42627, KCTD5, LOC100128788, LOC100507321, LOC652276, MIR3178, NTN3, PDPK1, PRSS27, SRRM2, TBC1D24
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv2570n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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