A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4132n100



Internal ID20155748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:187085330..187425784hg38UCSC Ensembl
chr2:187950057..188290511hg19UCSC Ensembl
chr2:187658302..187998756hg18UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg38340455
hg19340455
hg18340455
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1003061, nsv1000617
Samples
Known GenesCALCRL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4132n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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