A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7490n71



Internal ID6325110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:128458649..128560761hg19UCSC Ensembl
chr7:128245885..128347997hg18UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv889194, nsv889195, nsv889197, nsv889193
SamplesMS17208, IS32322, IS39233, MS18276, MS10769
Known GenesATP6V1F, CCDC136, FLNC, KCP, LOC100130705
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv7490n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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