A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4337n100



Internal ID22790424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:59878803..59931684hg38UCSC Ensembl
chr20:58453858..58506739hg19UCSC Ensembl
chr20:57887253..57940134hg18UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg3852882
hg1952882
hg1852882
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1064770, nsv1061189, nsv1059185, nsv1067289, nsv1059285, nsv1064279, nsv1055963, nsv1062636, nsv1063056, nsv1065356
Samples
Known GenesSYCP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4337n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss37
Observed Complex0
Frequencyn/a


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