A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4320n100



Internal ID20155936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:45713700..45758128hg38UCSC Ensembl
chr20:44342339..44386767hg19UCSC Ensembl
chr20:43775753..43820174hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3844429
hg1944429
hg1844422
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1065614, nsv1058632, nsv1066695
Samples
Known GenesSPINT4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4320n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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