A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4108n100



Internal ID22790195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:176290690..176360770hg38UCSC Ensembl
chr2:177155418..177225498hg19UCSC Ensembl
chr2:176863664..176933744hg18UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg3870081
hg1970081
hg1870081
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv998939, nsv1013703, nsv1006394, nsv1008093
Samples
Known GenesMTX2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4108n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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