A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1353n71



Internal ID6318973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:6929637..7007004hg19UCSC Ensembl
chr12:6799898..6877265hg18UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv898640, nsv898639
SamplesMS16153, MS18276
Known GenesCD4, CDCA3, DSTNP2, GNB3, GPR162, LEPREL2, RPL13P5, SPSB2, TPI1, USP5
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv1353n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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