A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5880n100



Internal ID22791967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:253272..385772hg38UCSC Ensembl
chr6:253272..385772hg19UCSC Ensembl
chr6:198272..330772hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38132501
hg19132501
hg18132501
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1026210, nsv1023143, nsv1019683, nsv1020641, nsv1022504, nsv1032862, nsv1018789, nsv1030229, nsv1027975, nsv1020233, nsv1033119, nsv1020522, nsv1022970, nsv1024083, nsv1019810, nsv1018834, nsv1015589, nsv1019071, nsv1028671, nsv1025386, nsv1025201, nsv1025121, nsv1024314, nsv1030418, nsv1019405, nsv1032203, nsv1030620, nsv1028547, nsv1021594, nsv1018436, nsv1018810, nsv1019731
Samples
Known GenesDUSP22
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5880n100
Frequency
Sample Size11257
Observed Gain161
Observed Loss327
Observed Complex0
Frequencyn/a


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