A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv184n71



Internal ID6317804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:17239973..17340878hg19UCSC Ensembl
chr1:17112560..17213465hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv871043, nsv871503
SamplesIS37646, MS17208
Known GenesATP13A2, CROCC, MFAP2
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv184n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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