A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4321n100



Internal ID22790408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:45719911..45754523hg38UCSC Ensembl
chr20:44348550..44383162hg19UCSC Ensembl
chr20:43781964..43816569hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3834613
hg1934613
hg1834606
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1059615, nsv1064805, nsv1055624, nsv1063907, nsv1056042, nsv1067142, nsv1059789, nsv1058268, nsv1059109, nsv1061414, nsv1065165, nsv1058573, nsv1067365, nsv1064018
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)dgv4321n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss138
Observed Complex0
Frequencyn/a


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