A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5894n100



Internal ID22791981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:314950..382559hg38UCSC Ensembl
chr6:314950..382559hg19UCSC Ensembl
chr6:259950..327559hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3867610
hg1967610
hg1867610
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1019604, nsv1030154, nsv1021334, nsv1015407, nsv1020094, nsv1033468
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)dgv5894n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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