A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4335n100



Internal ID22790422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:59844304..59936095hg38UCSC Ensembl
chr20:58419359..58511150hg19UCSC Ensembl
chr20:57852754..57944545hg18UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg3891792
hg1991792
hg1891792
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1063880, nsv1059132, nsv1066293, nsv1060589, nsv1059035, nsv1060714, nsv1065560, nsv1062840, nsv1059752, nsv1061522, nsv1055705, nsv1056705, nsv1056600, nsv1058271, nsv1063750
Samples
Known GenesFAM217B, PHACTR3, SYCP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4335n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss22
Observed Complex0
Frequencyn/a


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