A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5329n100



Internal ID20156945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:78793541..78867614hg38UCSC Ensembl
chr4:79714695..79788768hg19UCSC Ensembl
chr4:79933719..80007792hg18UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg3874074
hg1974074
hg1874074
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1011365, nsv1007685
Samples
Known GenesBMP2K
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5329n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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