A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2571n71



Internal ID6320191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2560161..2595303hg19UCSC Ensembl
chr16:2500162..2535304hg18UCSC 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 Variantsnsv905154, nsv905155, nsv905156
SamplesSP54043, SP54725, SP55021, SP51109
Known GenesAMDHD2, ATP6V0C, CEMP1, MIR3178, PDPK1
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv2571n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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