A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5957n100



Internal ID22792044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35534827..35611598hg38UCSC Ensembl
chr6:35502604..35579375hg19UCSC Ensembl
chr6:35610582..35687353hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3876772
hg1976772
hg1876772
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1026252, nsv1028721, nsv1023091, nsv1026200, nsv1020720, nsv1019593, nsv1021675, nsv1017625, nsv1025296, nsv1026532, nsv1022049, nsv1030879, nsv1028396, nsv1034413, nsv1021841, nsv1030461
Samples
Known GenesFKBP5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5957n100
Frequency
Sample Size11257
Observed Gain45
Observed Loss0
Observed Complex0
Frequencyn/a


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