A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4983n100



Internal ID20156599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:172746210..172823340hg38UCSC Ensembl
chr3:172464000..172541130hg19UCSC Ensembl
chr3:173946694..174023824hg18UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3877131
hg1977131
hg1877131
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1007382, nsv1000288
Samples
Known GenesECT2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4983n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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